Compass Pathways (NASDAQ: CMPS) reports strong positive Phase 3 TRD results

Filing Impact

(High)

Filing Sentiment

(Neutral)

Form Type

8-K

Rhea-AI Filing Summary

Compass Pathways reported strongly positive topline results from both pivotal Phase 3 trials of its COMP360 psilocybin treatment for treatment‑resistant depression. In COMP005, a single 25 mg dose showed a highly statistically significant mean MADRS improvement versus placebo of -3.6 points at Week 6 (p<0.001), with rapid onset from the day after dosing and durability out to Week 26 for many responders. In COMP006, two 25 mg doses given three weeks apart achieved a -3.8‑point difference versus 1 mg at Week 6 (p<0.001), with 39% of patients reaching a clinically meaningful ≥25% MADRS reduction. Across more than 800 treated patients in these Phase 3 arms, COMP360 was generally well-tolerated; most adverse events such as headache, nausea, anxiety and visual hallucinations occurred on dosing days and resolved within a day, and serious suicidal events were rare and mainly in lower‑dose or control arms. The company plans to meet the FDA to discuss rolling NDA submission and expects to complete an NDA for COMP360 in Q4, supported by Breakthrough Therapy designation.

Positive

Both pivotal Phase 3 TRD trials met primary endpoints, with COMP005 showing a -3.6 MADRS difference versus placebo and COMP006 showing a -3.8 difference versus 1 mg at Week 6 (both p<0.001), providing robust late-stage efficacy evidence for COMP360.
Clinically meaningful response and durability: 25% of COMP005 patients and 39% of COMP006 patients on 25 mg achieved ≥25% MADRS reduction at Week 6, with COMP005 responders maintaining benefit to at least Week 26 after one or two doses.
Regulatory momentum and clear path to filing: COMP360 holds FDA Breakthrough Therapy designation, the company plans an FDA meeting to discuss rolling NDA submission and review, and it expects to complete an NDA for COMP360 in Q4.
Generally well-tolerated safety profile: Most treatment-emergent adverse events (headache, nausea, anxiety, visual hallucinations) occurred on dosing days and resolved within a day, and serious adverse events, including suicidal ideation or behavior, were rare across both Phase 3 trials.

Negative

None.

Insights

Two positive Phase 3 TRD trials plus an NDA timeline make this a pivotal, clearly positive update.

Compass Pathways now has two independent Phase 3 trials in treatment‑resistant depression meeting their primary endpoints. COMP005 showed a -3.6 MADRS difference versus placebo at Week 6, while COMP006 showed a -3.8 difference for 25 mg versus 1 mg, both with p<0.001.

The data emphasize rapid onset (statistical separation the day after dosing) and meaningful durability. In COMP005, 25% of patients achieved a ≥25% MADRS reduction at Week 6 with benefits maintained to at least Week 26; in COMP006, 39% reached that response threshold at Week 6.

Safety appears manageable: adverse events were mostly transient and on dosing days, and serious suicidal events were infrequent and not concentrated in the high‑dose arm. With Breakthrough Therapy designation, plans for an FDA meeting on rolling review, and an NDA submission targeted for Q4, these results materially advance COMP360 toward potential approval in TRD.

02/17/2026 - 06:33 AM

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 OR 15(d) of the Securities Exchange Act of 1934

Date of report (Date of earliest event reported): February 17, 2026

COMPASS PATHWAYS PLC

(Exact Name of Registrant as Specified in Its Charter)



England and Wales	001-39522	Not applicable
(State or other Jurisdiction of Incorporation)	(Commission File Number)	(I.R.S. Employer Identification No.)

33 Broadwick Street

London W1F 0DQ

United Kingdom

(Address of Principal Executive Offices; Zip Code)

+1 (716) 676-6461

(Registrant’s Telephone Number, Including Area Code)

Not Applicable

(Former Name or Former Address, if Changed Since Last Report)

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:


			☐			Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
			☐			Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
			☐			Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
			☐			Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Trading

Symbol(s)

Name of each exchange on which registered

American Depositary Shares, each representing one ordinary share, nominal value £0.008 per share

CMPS

The Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐


Item 7.01			Regulation Fair Disclosure.

On February 17, 2026, Compass Pathways plc (the “Company” or "Compass") will be making an investor presentation (the "Presentation"). A copy of the Presentation is attached as Exhibit 99.1 to this Current Report on Form 8-K, and is incorporated herein by reference.

The information contained in Item 7.01 of this Current Report on Form 8-K, including Exhibit 99.1 attached hereto, is being furnished and shall not be deemed to be “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section and shall not be incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.


Item 8.01			Other Events.

On February 17, 2026, the Company announced the successful achievement of the primary endpoint in the ongoing Phase 3 COMP006 trial, the second of two Phase 3 trials, which is evaluating two fixed doses of COMP360, a synthetic, proprietary formulation of psilocybin, for treatment-resistant depression (TRD). The primary endpoint was the difference in change from baseline in the Montgomery-Åsberg Depression Rating Scale (MADRS) scores between the 25 mg and 1 mg groups at Week 6. Two fixed doses – administered 3 weeks apart – of COMP360 25 mg versus 1 mg demonstrated a highly statistically significant reduction in symptom severity with a p-value of <0.001 and a clinically meaningful difference of -3.8 points in change at the primary endpoint.

Across COMP005 and COMP006 to date, COMP360 is demonstrating a generally well-tolerated and safe profile, with treatment-emergent adverse events (TEAEs) being mild or moderate in severity, and the vast majority resolving within 24 hours. The data confirms a statistically significant rapid onset from the day following administration and maintained at all measured timepoints through Week 6 in both clinical trials in the 25 mg arm. COMP005 suggests that participants who demonstrated a clinically meaningful reduction in MADRS maintained durable treatment effect at least through Week 26, after just one or two doses. Retreatment with a second dose was well-tolerated, with a consistent safety profile.

Compass has submitted a request for a meeting with the U.S. Food and Drug Administration (FDA) to discuss a rolling submission and review.

Key Findings

Efficacy Profile

COMP005

•Primary endpoint of Part A (previously disclosed in June 2025): Single dose of COMP360 25 mg versus placebo with a mean treatment difference of -3.6 points, 95% CI [-5.7, -1.5]; p<0.001 at Week 64

•For participants who had a clinically meaningful reduction in MADRS (≥ 25%), a statistically significant rapid onset from the day following administration was maintained at all measured timepoints through Week 6 in the 25 mg arm

•25% of participants in the 25 mg arm achieved a clinically meaningful reduction in MADRS (≥ 25%) at Week 6 with durability lasting out through 26 weeks after just one or two doses of 25 mg

•Over 40% of those who achieved a clinically meaningful reduction in MADRS but had not remitted by 6 weeks went into remission after the second dose in Part B

COMP006

•Primary endpoint of Part A: Two doses of COMP360 25 mg versus 1 mg with a mean treatment difference of -3.8 points, 95% CI [-5.8, -1.8]; p<0.001 at Week 6

•39% of participants in the 25 mg arm achieved a clinically meaningful reduction in MADRS (≥ 25%) at Week 6

•For participants who achieved a clinically meaningful reduction in MADRS (≥ 25%), a statistically significant rapid onset from the day following administration was maintained at all measured timepoints through Week 6 in the 25 mg arm

•The 26-week data (Part B) from COMP006 is expected in early Q3 2026

Safety Profile

COMP005

In the 25 mg arm, (Part A and B):

•Most TEAEs occurred on the days of study drug administration (66%), with the vast majority (88%) resolving within a day

•Most common TEAEs reported were headache, nausea and visual hallucination

•There were 11 treatment-emergent serious adverse events (SAEs) from 8 participants (5%) overall

COMP006

In the 25 mg arm (Part A):

•Most TEAEs occurred on the days of study drug administration (73%) with the vast majority (83%) resolving within a day

•Most common TEAEs were headache, nausea, anxiety and visual hallucination

•There were 6 treatment-emergent serious adverse events (SAEs) from 6 participants (2%) overall

Across both trials, for the data available to date, the rate for SAE suicidal ideation was less than 1%. There was only one event of SAE suicidal behavior, which occurred in the 1 mg arm in COMP006.

The COMP360 program aims to evaluate the safety and efficacy of COMP360 psilocybin, a synthetic, proprietary formulation of psilocybin under investigation for difficult-to-treat mental health conditions. There are two pivotal Phase 3 trials, COMP005 and COMP006, evaluating the efficacy of COMP360 for treatment-resistant depression (TRD).

The ongoing COMP005 trial is a randomized, double-blind, placebo-controlled study, with 258 dosed participants across the United States and is assessing the efficacy and safety of a single dose of 25 mg COMP360 versus placebo for reducing symptom severity in TRD (COMP360 25 mg: n=171; placebo: n=87).The trial is comprised of three parts: Part A, which was blinded through 6 weeks; Part B, which has recently concluded and was blinded through week 26; and Part C, which contains an open-label treatment part from week 26 to 52.

The ongoing COMP006 trial, running in parallel to the COMP005 trial, is a randomized, double-blind study with 581 dosed participants across North America and Europe and is comparing the efficacy and safety of two fixed doses, taken three weeks apart, of 25 mg COMP360 to 10 mg COMP360 and 1 mg COMP360 (25 mg: n=296; 10 mg: n=142; 1 mg: n=143). The trial is comprised of three parts: Part A, which has recently concluded and was blinded through 9 weeks, Part B which remains blinded through week 26, and Part C, which contains an open-label treatment part from week 26 to 52.

Forward-Looking Statements

This Current Report on Form 8-K contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Any statements, other than statements of historical fact, including statements regarding the Company’s expectations regarding the safety or efficacy of its investigational COMP360 psilocybin treatment, including as a treatment for treatment of TRD or PTSD; the Company's plans and expectations regarding its clinical trials, including the Phase 3 trials in TRD and Phase 2b/3 trial in PTSD; the Company's expectations regarding the time periods for the release of data from Part B of the COMP006 Phase 3 trial for TRD; the Company's expectations regarding its discussions with the FDA, including discussions regarding potential NDA acceleration strategies, including potential for rolling NDA submission and review for COMP360 psilocybin treatment in TRD; the potential for the pivotal Phase 3 program in TRD to support regulatory filings and approvals; any implication that past results will be predictive of future results; and any other statements containing the words “expects,” “anticipates,” “plans,” and similar expressions, are forward-looking statements. These forward-looking statements are based on the Company’s current intentions, beliefs and expectations regarding future events. The Company cannot guarantee that any forward-looking statement will be accurate. Investors should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could differ materially from the Company’s expectations, including uncertainties associated with risks related to clinical development which is a lengthy and expensive process with uncertain outcomes, and therefore the Company’s clinical trials may be delayed or terminated and may be more costly than expected; the full results and safety data from the Phase 3 clinical trials in TRD may not be consistent with the preliminary results to date; the Company's acceleration strategies for its NDA submission may not be successful; FDA may ultimately disagree with the Company's proposal for a rolling NDA submission and may not permit us to utilize the rolling review process; the Company's efforts to obtain marketing approval from FDA or regulatory authorities in any other jurisdiction for the Company's investigational COMP360 psilocybin treatment may be unsuccessful; and those risks and uncertainties

described under the heading “Risk Factors” in the Company’s most recent annual report on Form 10-K or quarterly report on Form 10-Q and in other reports the Company has filed with the U.S. Securities and Exchange Commission (“SEC”), which are available on the SEC’s website at www.sec.gov. Investors are, therefore, cautioned not to place undue reliance on any forward-looking statement. Any forward-looking statement speaks only as of the date of this Form 8-K, and, except as required by law, the Company does not undertake to update any forward-looking statement to reflect new information, events or circumstances.


Item 9.01.			Financial Statements and Exhibits.


(d)			Exhibits.


Exhibit No.						Description

99.1						Investor Presentation dated February 17, 2026.
104						Cover page interactive data file (embedded within Inline XBRL document)

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

COMPASS PATHWAYS PLC

Date: February 17, 2026

By:

/s/ Teri Loxam

Teri Loxam

Chief Financial Officer

1 | © Compass Pathways COMP360 Phase 3 Program Topline Results COMP005 & COMP006 February 17, 2026

2 | © Compass Pathways Cautionary Note Regarding Forward-Looking Statements This presentation includes “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. In some cases, you can identify forward-looking statements by terms such as “believe,” “continue,” “could,” “estimate,” “expect,” “may,” “might,” “plan,” “potential,” “project,” “target,” “will,” “would,” or the negative of these terms, and similar expressions intended to identify forward-looking statements. However, not all forward-looking statements contain these identifying words. These forward-looking statements include express or implied statements relating to, among other things, statements regarding our business strategy and goals; our expectations and projections about the company’s future cash needs and financial results; our expectations regarding the safety or efficacy of our investigational COMP360 psilocybin treatment, including as a treatment for treatment of TRD or PTSD; our plans and expectations regarding our clinical trials, including our phase 3 trials in TRD and our phase 2b/3 trial in PTSD; our expectations regarding the time periods for the release of data from Part B of the COMP006 Phase 3 trial for TRD; our expectations regarding discussions with the FDA, including discussions regarding potential NDA acceleration strategies, including potential for rolling NDA submission and review for COMP360 psilocybin treatment in TRD; our expectations regarding potential commercial launch timelines and our commercial readiness; the potential for the pivotal phase 3 program in TRD to support regulatory filings and approvals on an accelerated basis or at all; our ability to obtain regulatory approval and adequate coverage and reimbursement; our ability to transition from a clinical-stage to a commercial-stage organization and effectively launch a commercial product, if regulatory approval is obtained, on an accelerated timeline or at all; our expectations regarding the commercial potential for COMP360 and our expectations regarding the benefits of our investigational COMP360 psilocybin treatment. The forward-looking statements in this press release are neither promises nor guarantees, and you should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties, and other factors, many of which are beyond Compass’s control and which could cause actual results, levels of activity, performance or achievements to differ materially from those expressed or implied by these forward-looking statements. These risks, uncertainties, and other factors include, among others: uncertainties associated with risks related to clinical development which is a lengthy and expensive process with uncertain outcomes, and therefore our clinical trials may be delayed or terminated and may be more costly than expected; the full results and safety data from our Phase 3 clinical trials in TRD may not be consistent with the preliminary results to date; our need for substantial additional funding to achieve our business goals and if we are unable to obtain this funding when needed and on acceptable terms, we could be forced to delay, limit or terminate our clinical trials; our acceleration strategies for our NDA submission may not be successful; FDA may ultimately disagree with our proposal for a rolling NDA submission and may not permit us to utilize the rolling review process; our efforts to obtain marketing approval from FDA or regulatory authorities in any other jurisdiction for our investigational COMP360 psilocybin treatment may be unsuccessful; our efforts to commercialize and obtain coverage and reimbursement for our investigational COMP360 psilocybin treatment, if approved, may be unsuccessful; the risk that our strategic collaborations will not continue or will not be successful; and our ability to retain key personnel; and those risks and uncertainties described under the heading “Risk Factors” in Compass’s most recent annual report on Form 10-K or quarterly report on Form 10-Q, and in other reports we have filed with the U.S. Securities and Exchange Commission (“SEC”), which are available on the SEC’s website at www.sec.gov. You should not rely upon forward-looking statements as predictions of future events. Although our management believes that the expectations reflected in our statements are reasonable, we cannot guarantee that the future results, levels of activity, performance or events and circumstances described in the forward-looking statements will be achieved or occur. Moreover, neither we, nor any other person, assumes responsibility for the accuracy and completeness of these statements. Accordingly, you are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date such statements are made and should not be construed as statements of fact. Except as required by applicable law, we undertake no obligation to update these forward-looking statements to reflect any new information, events or circumstances after the date hereof, or to reflect the occurrence of unanticipated events. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements. Market & Industry Data Market & industry data projections, estimates, industry data and information contained in this presentation, including our general expectations about our market position and market opportunity, are based on information from third-party sources, publicly available information, our knowledge of our industry and assumptions based on such information and knowledge. Although we believe that our third party-sources are reliable, we cannot guarantee the accuracy or completeness of our sources. All of the projections, estimates, market data and industry information used in this presentation involve a number of assumptions and limitations, and you are cautioned not to give undue weight to such information. In addition, projections, estimates and assumptions relating to our and our industry’s future performance are necessarily subject to a high degree of uncertainty and risk due to a variety of factors, including, but not limited to, those described above, that could cause future performance to differ materially from our expressed projections, estimates and assumptions or those provided by third parties. Disclaimer

3 | © Compass Pathways Welcome Kabir Nath Chief Executive Officer Dr Guy Goodwin Chief Medical Officer Lori Englebert Chief Commercial Officer

4 | © Compass Pathways Tremendous Unmet Need in Treatment Resistant Depression (TRD) >4M U.S. adults experiencing TRD each year1 Only 1 Medicine approved and used for TRD High Patient Burden vs. MDD • Chronic condition • Increased co-morbidities • 3x longer episodes2 • Greater worktime loss3 • >50% increased risk of suicide4 • Poorer quality of life • Disproportionate economic impact5 1. Data on file; 2. Wu B, et al. PLoS One. 2019;14(8):e0220763. 3. Amos TB, et al. J Clin Psychiatry. 2018;79(2):17m11725. 4. Gustafsson TT, et al. J Affect Disord. 2025;368:136-142.; 5. Zhdanava, M., et. al; The Prevalence and National Burden of Treatment-Resistant Depression and Major Depressive Disorder in the United States. The Journal of clinical psychiatry, 82(2), 20m13699. https://doi.org/10.4088/JCP.20m13699

5 | © Compass Pathways Phase 3 Program Key Highlights • Two highly statistically significant positive Phase 3 trials of COMP360 in TRD at primary endpoint* at Week 6 - Over 1,000 participants across Phase 3 trials and Phase 2b trial - Both Phase 3 trials continuing to 52 weeks • Extremely rapid onset with statistical significance demonstrated from the day immediately following administration and maintained at all measured timepoints through Week 6 in both clinical trials • Deep and durable response achieved in significant number of participants • 25% of participants in 005 achieved a clinically meaningful reduction in MADRS** at Week 6 with durability lasting out through at least 26 weeks after just 1 or 2 doses of 25 mg • Over 40% of those that had a clinically meaningful reduction in MADRS but had not remitted by Week 6 went into remission after 2nd dose in 005 Part B • 39% of participants in 006 achieved clinically meaningful reduction in MADRS at Week 6 • COMP360 has been generally well-tolerated, with a safe profile, with majority of AEs resolving on the day of treatment *Primary endpoint for both trials is the change from baseline in the MADRS (Montgomery-Åsberg Depression Rating Scale) total score at Week 6. **Clinically meaningful reduction in MADRS defined as a >25% reduction from baseline in MADRS total score

6 | © Compass Pathways Phase 3 Program Key Highlights (cont’d) • The emerging clinical profile of COMP360 is redefining rapidity and durability for TRD patients - No approved drug offers clinically meaningful efficacy with both rapid onset and sustained durability with a single treatment • The robust benefit/risk profile of COMP360 supports a potentially highly compelling, novel paradigm for patients and providers where effectiveness may be determined almost immediately after a single treatment - Patients with a clinically meaningful reduction in MADRS to the first treatment have shown the potential for sustained benefit through at least 26 weeks, after one or two doses • COMP360 has Breakthrough Therapy designation from the FDA and we are planning to meet as soon as possible with the FDA to discuss a rolling submission and review, and expect to complete an NDA submission in Q4

7 | © Compass Pathways Phase 3 Trial Design and Demographics

8 | © Compass Pathways Phase 3 Program: Overview of Pivotal Trial Designs Pivotal trial 1 (COMP 005) single dose N=258 COMP360 25 mg N=171 Pivotal trial 2 (COMP 006) multiple dose N=581 COMP360 25 mg N=296 COMP360 1 mg N=143 COMP360 25 mg COMP360 1 mg COMP360 10 mg N=142 COMP360 10 mg Week 3 Week 6 Primary endpoint achieved1 option for retreatment* based on pre-specified criteria (same dose as Part A) COMP360 25mg treatment (one dose only after relapse or for non-remitters from Part B) Part A (blinded) 6 weeks Part B (blinded) 20 weeks Part C (open label) 26 weeks Placebo N=87 option for retreatment* based on pre-specified criteria (same dose as Part A) COMP360 25mg treatment (one dose only after relapse or for non-remitters from Part B) Part A (blinded) 9 weeks Part B (blinded) 17 weeks Part C (open label) 26 weeks 1. Primary endpoint = change from baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) total score at Week 6. Week 9 Key secondary endpoint Week 6 Primary endpoint achieved1 *Re-dosing for non-remitters from Part A or Part B could occur several weeks after transition to Part B or Part C, respectively, due to scheduling requirements. Participants were permitted to take protocol-allowed antidepressant treatments in Part B and C of the study.

9 | © Compass Pathways Placebo (N=87) COMP360 25 mg (N=171) COMP005 47 (54.0)93 (54.4)Female, n (%) Race, n (%) 78 (89.7)149 (87.1)White 4 (4.6)11 (6.4)Asian 2 (2.3)6 (3.5)Black or African American 1 (1.1)0American Indian or Alaska Native 2 (2.3)5 (2.9)Other 45.3 (14.4)45.9 (13.4)Age, years, mean (SD) 22, 7219, 77Min, Max 11 (12.6)15 (8.8)Age ≥65 years old 5 (5.7)5 (2.9)Prior psilocybin experience, n (%) 6 (6.9)8 (4.7)Prior psychedelic experience including psilocybin, n (%)* 27.7 (6.1)28.4 (6.2)BMI kg/m2 , mean (SD) *planned limit was 15% BMI = Body Mass Index; n=number of observed participants; SD = standard deviation COMP005 & COMP006 – Participant Baseline Demographics In Line with Known TRD Epidemiology COMP360 1 mg (N=143) COMP360 10 mg (N=142) COMP360 25 mg (N=296) COMP006 69 (48.3)68 (47.9)160 (54.1)Female, n (%) Race, n (%) 129 (90.2)123 (86.6)255 (86.1)White 6 (4.2)6 (4.2)14 (4.7)Asian 4 (2.8)3 (2.1)8 (2.7)Black or African American 1 (0.7)00American Indian or Alaska Native 3 (2.1)10 (7.0)19 (6.4)Other/not reported 45.5 (13.1)42.9 (12.8)46.2 (13.7)Age, years, mean (SD) 20, 7519, 7318, 79Min, Max 13 (9.1)9 (6.3)29 (9.8)Age ≥65 years old 5 (3.5)5 (3.5)13 (4.4)Prior psilocybin experience, n (%) 9 (6.3)7 (4.9)19 (6.4)Prior psychedelic experience including psilocybin, n (%) 27.8 (6.7)28.6 (7.1)28.0 (6.2)BMI kg/m2 , mean (SD)

10 | © Compass Pathways MADRS = Montgomery-Åsberg Depression Rating Scale; n=number of observed participants; SD = standard deviation. Placebo (N=87) COMP360 25 mg (N=171) COMP005 Number of failed treatments in the current depressive episode, n (%) 1 (1.1)2 (1.2)1 63 (72.4)113 (66.1)2 18 (20.7)46 (26.9)3 4 (4.6)10 (5.8)4 1 (1.1)05 Number of treatments withdrawn from the screening period, n (%) 26 (29.9)58 (33.9)0 32 (36.8)38 (22.2)1 22 (25.3)49 (28.7)2 7 (8.0)26 (15.2)>2 31.5 (5.9)31.5 (5.5)MADRS total score at baseline, mean (SD) MADRS total score severity at baseline, n (%) 2 (2.3)1 (0.6)Mild (11-19) 33 (37.9)73 (42.7)Moderate (20-30) 52 (59.8)97 (56.7)Severe (≥31) COMP005 & COMP006 – Participant Characteristics Treatment History and Baseline MADRS COMP360 1 mg (N=143) COMP360 10 mg (N=142) COMP360 25 mg (N=296) COMP006 Number of failed treatments in current depressive episode, n (%) 01 (0.7)1 (0.3)1 99 (69.2)105 (73.9)190 (64.2)2 33 (23.1)32 (22.5)74 (25.0)3 11 (7.7)4 (2.8)29 (9.8)4 002 (0.7)5 Number of treatments withdrawn from the screening period, n (%) 36 (25.2)31 (21.8)68 (23.0)0 62 (43.4)61 (43.0)127 (42.9)1 31 (21.7)35 (24.6)68 (23.0)2 14 (9.8)15 (10.6)33 (11.1)>2 32.5 (5.4)32.1 (5.8)32.0 (5.8)MADRS total score at baseline, mean (SD) MADRS total score severity at baseline, n (%) 002 (0.7)Subthreshold ≤10 000Mild (11-19) 49 (34.3)54 (38.0)115 (38.9)Moderate (20-30) 94 (65.7)88 (62.0)179 (60.5)Severe (≥31)

11 | © Compass Pathways n=number of observed participants; SD = standard deviation Placebo (N=87) COMP360 25 mg (N=171) COMP005 Length of current depressive episode 38.6 (33.0)34.6 (30.1)Mean Months (SD) 20 (23.0)30 (17.5)< 1 year 19 (21.8)52 (30.4)1-2 years 48 (55.2)89 (52.0)>2 years Number of lifetime depressive episodes 7.2 (7.6)7.7 (10.9)Mean (SD) 54 (62.1)107 (62.6)2-5 21 (24.1)40 (23.4)6-10 12 (13.8)23 (13.5)>10 COMP005 & COMP006 – Participant Characteristics Depression Diagnosis History COMP360 1 mg (N=143) COMP360 10 mg (N=142) COMP360 25 mg (N=296) COMP006 Length of current depressive episode 38.4 (45.0)37.7 (38.8)45.5 (42.7)Mean Months (SD) 30 (21.0)37 (26.1)53 (17.9)< 1 year 41 (28.7)35 (24.6)73 (24.7)1-2 years 72 (50.3)70 (49.3)170 (57.4)>2 years Number of lifetime depressive episodes 7.0 (12.5)5.4 (6.6)6.3 (7.4)Mean (SD) 001 (0.3)1 99 (69.2)109 (76.8)198 (66.9)2-5 30 (21.0)21 (14.8)61 (20.6)6-10 10 (7.0)10 (7.0)29 (9.8)>10

12 | © Compass Pathways COMP005 Efficacy Data

13 | © Compass Pathways COMP005 - Primary Endpoint Achieved – Change in MADRS at Week 6 CI = Confidence Interval; LSM = Least Squares Mean; MADRS = Montgomery–Åsberg Depression Rating Scale; SD=standard deviation. LS Mean Difference (95% CI) P-value Visit -4.7 (-7.0, -2.3), p<0.001 Day 2 -7.2 (-9.6, -4.8), p<0.001 Week 1 -5.2 (-7.4, -2.9), p<0.001 Week 3 -3.6 (-5.7, -1.5), p<0.001 Week 6 (Primary) • Highly statistically significant difference of -3.6 MADRS between 25mg vs placebo at Week 6 (p<0.001) • Statistical significance at all timepoints beginning the day after administration (Day 2) demonstrates rapid onset of action Baseline mean (SD): 25 mg (n=171) = 31.5 (5.5) Placebo (n=87) = 31.5 (5.9) -4.9 (-6.3, -3.4) -1.2 (-3.3, 0.8) -1.8 (-3.9, 0.3) -7.0 (-8.5, -5.4) -9.9 (-11.5, -8.2) -2.6 (-4.9, -0.4) -5.0 (-7.2, -2.8) -9.7 (-11.2, -8.1)

14 | © Compass Pathways COMP005 – Sustained Durability to Week 26 Source: Post Hoc (Include Number) Note: : CI = Confidence Interval; LSM = Least Squares Mean; MADRS = Montgomery–Åsberg Depression Rating Scale. • Consistent separation from placebo through randomized and blinded part B up to Week 26 • Option for 2nd administration* of COMP360 after Week 6 during blinded long-term follow-up (Part B) • 70% of patients in 25mg arm and 53% in placebo arm received a 2nd administration after Week 6 -14 -12 -10 -8 -6 -4 -2 0 2 Baseline (Day -1) Day 2 Week 1 Week 3 Week 6 Le as t sq u ar e m ea n (± 95 % C Is ) c h an g e fr o m B as e lin e Week 10 Week 14 Primary Endpoint at Week 6 No statistical analyses performed after the primary analysis at Week 6 Week 18 Week 22 Week 26 2nd administration option during blinded long- term follow-up through Week 26 (Part B) *2nd administration based on pre-specified criteria and receive either what they were randomized into or antidepressant CI = Confidence Interval; LSM = Least Squares Mean; MADRS = Montgomery–Åsberg Depression Rating Scale

15 | © Compass Pathways Definitions (n at Week 6): Remitters (n=11) = MADRS ≤12 and no single item ≥4 Responders and Partial Responders (n=31) = % CFB in MADRS ≥ 25% and do not meet remission criterion Non-Responder (n=115) = % CFB in MADRS ≤ 25% Total n at 6 weeks = 157 (8% dropout) *Clinically meaningful reduction in MADRS defined as a >25% reduction from baseline in MADRS total score at Week 6. This graph is a post hoc analysis. CI = Confidence Interval; CFB = change from baseline; MADRS = Montgomery–Åsberg Depression Rating Scale • 25% of participants in 25mg arm achieved clinically meaningful reduction in MADRS* at Week 6 and maintained response at least through Week 26 • Magnitude of MADRS improvement among responders demonstrates consistent, durable and clinically meaningful effect • Over 40% of those who achieved clinically meaningful reduction in MADRS but had not remitted by 6 weeks went into remission after 2nd dose in Part B COMP005 – Durability Through Week 26 by Response Status >25% reduction in MADRS

17 | © Compass Pathways -14 -12 -10 -8 -6 -4 -2 0 COMP360 25 mg (N=296) COMP360 10 mg (N=142) COMP360 1 mg (N=143) 10mg vs 1 mg LS Mean Difference (95% CI) P-value 25mg vs 1 mg LS Mean Difference (95% CI) P-value Visit -3.0 (-5.0, -1.0) 0.002 -2.9 (-4.6, -1.2) <0.001 Day 2 -3.6 (-5.9, -1.2) 0.001 -5.0 (-7.0, -3.0) <0.001 Week 1 -3.4 (-5.6, -1.2) 0.001 -4.5 (-6.4, -2.5) <0.001 Week 3 -4.9 (-7.4, -2.4) <0.001 -5.0 (-7.1, -2.9) <0.001 Day 24 -4.9 (-7.3, -2.5) <0.001 -4.8 (-6.9, -2.7) <0.001 Week 4 -2.5 (-4.9, -0.2) 0.016 -3.8 (-5.8, -1.8) <0.001 Week 6 (Primary) • Statistically significant difference of -3.8 MADRS between 25mg vs 1mg at Week 6 (p<0.001) • Statistically significant treatment differences in 25mg vs 1mg and 10mg vs 1 mg found at all timepoints post administration • Rapid onset of action with the effect occurring the day after the administration (Day 2) • 39% of participants in 25mg arm achieved a clinically meaningful reduction in MADRS at Week 6* Baseline mean (SD): 25 mg (n=296) = 32.0 (5.8) 10 mg (n=142) = 32.1 (5.8) 1 mg (n=143) = 32.5 (5.4) Baseline (Day -1) Day 2 Week 1 Week 3 Day 24 Week 4 Week 6 -7.6; (-8.8, -6.4) Le as t sq u ar e m ea n (± 95 % C Is ) c h an g e fr o m B as e lin e -6.3; (-8.0, -4.6) -3.7; (-5.4, -2.1) *Clinically meaningful reduction in MADRS defined as a >25% reduction from baseline in MADRS total score at Week 6 CI = Confidence Interval; LSM = Least Squares Mean; MADRS = Montgomery–Åsberg Depression Rating Scale COMP006 – Primary Endpoint Met – Change in MADRS at Week 6

18 | © Compass Pathways CI = Confidence Interval; LSM = Least Squares Mean; MADRS = Montgomery–Åsberg Depression Rating Scale. 10mg vs 1 mg LS Mean Difference (95% CI) P-value 25mg vs 1 mg LS Mean Difference (95% CI) P-value Visit -2.5 (-4.9, -0.2) 0.016 -3.8 (-5.8, -1.8) <0.001 Week 6 (Primary) -2.6 (-5.0, -0.2) 0.016 -2.9 (-5.0, -0.9) 0.002 Week 9 (Secondary) • Statistical significance maintained through Week 9 -14 -12 -10 -8 -6 -4 -2 0 COMP360 25 mg (N=296) COMP360 10 mg (N=142) COMP360 1 mg (N=143) Baseline (Day -1) Day 2 Week 1 Week 3 Week 9 Day 24 Week 4 Week 6 -7.6; (-8.8, -6.4) Le as t sq u ar e m ea n (± 95 % C Is ) c h an g e fr o m B as e lin e -6.3; (-8.0, -4.6) -3.7; (-5.4, -2.1) -2.7; (-4.4, -1.0) -5.3; (-7.0, -3.6) -5.6; (-6.8, -4.4) COMP006 – Key Secondary Met – Change in MADRS at Week 9

19 | © Compass Pathways COMP005 & COMP006 Primary Endpoint Comparison* *Cross-trial comparisons should be interpreted with caution. Differences between these trials, including but not limited to study designs, protocols, timing of assessments, number or timing of doses and participant populations can meaningfully influence outcomes and limit the validity of any comparison. CI = Confidence Interval; LSM = Least Squares Mean; MADRS = Montgomery–Åsberg Depression Rating Scale -14 -12 -10 -8 -6 -4 -2 0 2 COMP360 25 mg (COMP 006) (N=296) COMP360 1 mg (COMP 006) (N=143) COMP360 25 mg (COMP 005) (N=171) Placebo (COMP 005) (N=87) Baseline (Day -1) Day 2 Week 1 Week 3 Day 24 Week 4 Week 6 Le as t sq u ar e m ea n (± 95 % C Is ) c h an g e fr o m B as e lin e  3.6  3.8 2nd dose in 006 trial • Consistent magnitude of MADRS total score improvement between two Phase 3 studies • 2nd administration at Week 3 shows potential for a deeper treatment effect than a single administration

21 | © Compass Pathways Safety Summary • COMP360 is generally well-tolerated, with a safe profile, with the majority of AEs resolving on day of treatment • Safety data is consistent with known safety profile of COMP360 – no new safety signals identified • For the data available to date across both trials, the rate for SAE suicidal ideation was less than 1%. There was only one event of SAE suicidal behavior, which occurred in the 1 mg arm in COMP006. - To date there have been no attempted or completed suicides • The DSMB noted that there is no evidence of a clinically meaningful imbalance between treatment arms in suicidality in either study COMP005: In 25 mg arm (Part A and B): • Most TEAEs occurred on the days of administration (66%), with the vast majority (88%) resolving within a day • Most common TEAEs reported were headache, nausea and visual hallucination • There were 11 treatment-emergent serious adverse events (SAEs) from 8 participants (5%) overall COMP006: In 25 mg arm (Part A): • Most TEAEs occurred on the days of administration (73%) with the vast majority (83%) resolving within a day • Most common TEAEs were headache, nausea, anxiety and visual hallucination • There were 6 treatment-emergent serious adverse events (SAEs) from 6 participants (2%) overall

22 | © Compass Pathways N=number of participants in the treatment group in the Safety Analysis Set by administration; n = number of participants; TEAE = treatment emergent adverse event PlaceboCOMP360 25 mg COMP005 N=87N=171 n (%) n (%) 34 (39.1)120 (70.2)Any TEAE up to Week 6 1 (1.1)4 (2.3)Any Serious TEAE up to Week 6 23 (26.4)118 (69.0)Any TEAE time of onset day of dosing 22 (25.3)111 (64.9)Resolved ≤ 1 Day 2 (2.3)15 (8.8)Resolved > 1 and ≤ 2 Days 5 (5.7)22 (12.9)Resolved > 2 Days COMP360 1 mg COMP360 10 mg COMP360 25 mg COMP006 N=143N=142N=296 n (%)n (%) n (%) 116 (81.1)125 (88.0)274 (92.6)Any TEAE up to Week 9 5 (3.5)1 (0.7)6 (2.0)Any Serious TEAE up to Week 9 80 (55.9)114 (80.3)260 (87.8)Any TEAE with onset on day of dosing 71 (49.7)107 (75.4)244 (82.4)Resolved ≤ 1 Day 9 (6.3)16 (11.3)52 (17.6)Resolved > 1 and ≤ 2 Days 20 (14.0)26 (18.3)71 (24.0)Resolved > 2 Days Note: COMP006 safety includes 2 dose administrations and goes out to 9 weeks vs. 1 administration out to 6 weeks for COMP005 COMP005 & COMP006 Treatment-Emergent Adverse Events (TEAEs) for Part A

23 | © Compass Pathways MedDRA = Medical Dictionary for Regulatory Activities; N=number of participants in the treatment group in the Safety Analysis Set by administration; n = number of participants. PlaceboCOMP360 25 mgCOMP005 (>5% Incidence) MedDRA TEAE Preferred Term N=87N=171 n (%) n (%) 12 (13.8)86 (50.3)Any TEAE 10 (11.5)42 (24.6)Headache 3 (3.4)35 (20.5)Nausea 024 (14.0)Hallucination, visual 2 (2.3)14 (8.2)Anxiety 2 (2.3)10 (5.8)Dizziness 1 (1.1)9 (5.3)Illusion COMP360 1 mgCOMP360 10 mgCOMP360 25 mgCOMP006 (>10% Incidence) MedDRA TEAE Preferred Term N=143N=142N=296 n (%)n (%) n (%) 80 (55.9)111 (78.2)254 (85.8)Any TEAE 15 (10.5)42 (29.6)118 (39.9)Nausea 41 (28.7)43 (30.3)108 (36.5)Headache 21 (14.7)28 (19.7)62 (20.9)Anxiety 3 (2.1)24 (16.9)46 (15.5)Hallucination, visual 3 (2.1)16 (11.3)41 (13.9)Illusion 9 (6.3)21 (14.8)41 (13.9)Dizziness 16 (11.2)23 (16.2)41 (13.9)Fatigue 4 (2.8)13 (9.2)35 (11.8)Crying 4 (2.8)6 (4.2)31 (10.5)Blood pressure increased Note: COMP006 safety includes 2 dose administrations and goes out to 9 weeks vs. 1 administration out to 6 weeks for COMP005 COMP005 & COMP006 Treatment-Emergent Adverse Events (TEAE) Incidence for Part A

24 | © Compass Pathways n = number of participants with TESAE; TESAE = treatment emergent serious adverse event COMP360 1 mg COMP360 10 mg COMP360 25 mg COMP006 N=143N=142N=296 n (%)n (%) n (%) 5 (3.5)1 (0.7)6 (2.0)Any SAE 2 (1.4)1 (0.7)0Suicidal ideation 1 (0.7)00Suicidal behaviour 1 (0.7)01 (0.3)Syncope 001 (0.3)Major depression 001 (0.3)Anxiety 001 (0.3)Flashback 001 (0.3)Cervical spinal stenosis 1 (0.7)00Renal neoplasm 001 (0.3)Pelvic pain PlaceboCOMP360 25 mg COMP005 N=87N=171 n (%) n (%) 1 (1.1)4 (2.3)Any SAE 02 (1.2)Suicidal ideation 01 (0.6)Depression suicidal 1 (1.1)0Major depression 01 (0.6)Cellulitis 01 (0.6)Diverticulitis Note: COMP006 safety includes 2 dose administrations and goes out to 9 weeks vs. 1 administration out to 6 weeks for COMP005 COMP005 & COMP006 Treatment-Emergent Serious Adverse Events (SAEs) for Part A

25 | © Compass Pathways COMP005 – Safety Data Through Week 26 TEAEs MedDRA = Medical Dictionary for Regulatory Activities; N=number of participants in the treatment group in the Safety Analysis Set by administration; n = number of participants. Table shows TEAEs occurring in ≥ 5% in each treatment period. Placebo COMP360 25 mgMedDRA TEAE Preferred Term N=87N=171 n (%) n (%) 2 (2.3)8 (4.7)Any TESAE 04 (2.3)Suicidal ideation 01 (0.6)Depression suicidal 1 (1.1)0Major depression 01 (0.6)Cellulitis 01 (0.6)Diverticulitis 1 (1.1)0Urinary tract infection bacterial 01 (0.6)Clavicle fracture 01 (0.6)Rib fracture 01 (0.6)Pneumothorax 01 (0.6)Anaphylactic reaction SAEs PlaceboCOMP360 25 mgMedDRA TEAE Preferred Term N=87N=171 n (%) n (%) 23 (26.4)111 (64.9)Any TEAE 15 (17.2)61 (35.7)Headache 4 (4.6)42 (24.6)Nausea 027 (15.8)Hallucination, visual 3 (3.4)22 (12.9)Anxiety 2 (2.3)14 (8.2)Dizziness 1 (1.1)11 (6.4)Illusion 3 (3.4)9 (5.3)Blood pressure increased 3 (3.4)9 (5.3)Insomnia

27 | © Compass Pathways ~23M ~4M ~12M The definition of TRD adopted by the US Food and Drug Administration (FDA) is failure to respond to two or more antidepressant regimens despite adequate dose and duration and adherence to treatment3TRD 1.. https://www.nimh.nih.gov/health/statistics/major-depression Accessed June 21, 2025. 2. Data on file. 3. US Food and Drug Administration. Major Depressive Disorder (MDD): Developing Drugs for Treatment. Guidance for Industry. June 2018. https://www.fda.gov/media/113988/download. Accessed May 21, 2025. Over 55 medicines approved for MDD Only 2 medicines approved for TRD and only one that is used , Spravato® Prevalence of U.S. adults experiencing major depression each year1 Treatment-Resistant Depression (TRD) Affects Millions in the U.S. Adult patients who are drug treated for MDD in the past year2 MDD patients failed by ≥2 antidepressants and considered TRD2

28 | © Compass Pathways 1. Wu B, et al. PLoS One. 2019;14(8):e0220763. 2. Amos TB, et al. J Clin Psychiatry. 2018;79(2):17m11725. 3. Gustafsson TT, et al. J Affect Disord. 2025;368:136-142. TRD has a significantly greater impact on individuals’ lives compared to MDD Patients with TRD have longer depressive episodes1 17-30% increased risk of all-cause mortality3 70% greater work time loss2 51% increased risk of mortality due to suicide3 1st MDD episode 1st TRD episode 571 6005004003002001000 Days 200 Compared to patients with non-TRD MDD, those with TRD experience: lighter color = MDD darker color = TRD

29 | © Compass Pathways TRD Disproportionately Impacts the Annual Economic Burden of MDD ~$93B Annual Economic Burden of drug-treated MDD1 1. Zhdanava, M., et. al; The Prevalence and National Burden of Treatment-Resistant Depression and Major Depressive Disorder in the United States. The Journal of clinical psychiatry, 82(2), 20m13699. https://doi.org/10.4088/JCP.20m13699 TRD is associated with disproportionate health care costs and unemployment, suggesting potentially large economic and societal gains with effective management1 Non-TRD MDD 53% TRD 47% 1/3rd of MDD patients are failed by ≥2 antidepressants and considered treatment resistant1

30 | © Compass Pathways Potentially Highly Differentiated and Compelling COMP360 Clinical Profile for TRD Patients and their Providers Traditional AntidepressantsSpravato®COMP3601 NoYes (FDA approved) Yes (Positive trials: 2 ph3 trials; 1 ph2b)Efficacy in TRD patient population2 Various: typically change from baseline in MADRS at Week 6 vs. placebo Change from baseline in MADRS at Day 28 TRANSFORM 2: Esk+AD vs. Pbo+AD Change from baseline in MADRS at Week 6 005: 25mg vs. Pbo 006: 25mg vs. 1mg Primary Endpoint Varies: Recent treatment approved = -3.8 (p=.002)6TRANSFORM 2: -4.0 (p=0.02)4005: -3.6 (p<0.001) 006: -3.8 (p<0.001)Effect Size / p-value Avg 2 - 8 weeksStat sig at day 28 (adj)4Stat sig day after dosingOnset Daily dosing Induction: 2x/week in month 1 Maintenance: 1x/week in month 2, then every 1 or 2 weeks4 At least 26 weeks after 1 or 2 doses3Durability Generally safe but chronic side effects commonGenerally well-tolerated & safeGenerally well-tolerated and safe profileSafety & Tolerability Various: oral tablet or capsules QD or BID 56mg or 86mg intranasal; 2 or 3 devices / administration 25mg oral capsule; 1 capsule / administrationDose and Administration n/aAt least 2 hours post administration by licensed HCP at certified center At least 6hrs post administration by licensed HCP at certified centerMonitoring ~12M7<100,000 patients5n/a# of Patients Treated annually n/a$1.5B5n/a2025 Revenue 1. As demonstrated through COMP005 Part A and Part B and COMP006 Part A clinical trial top line results; final profile will depend on FDA approval and label; expectations at this time 2. As proven through clinical trials specifically for a TRD patient population; COMP360 remains investigational and has not been approved by FDA or any other regulatory authority 3. For those who achieved clinically meaningful reduction in MADRS: ≥ 25% reduction from baseline in MADRS total score 4. Spravato® Prescribing Information and www.spravatohcp.com; For appropriateness, only comparing trials run prior to FDA approval (TRANSFORM 1 and 2) 5. IQVIA data for 2024 # of patients treated and J&J 2025 Q4 earnings call 6. Data on file 7. www.auvelityhcp.com Note: No head to head studies between COMP360 and Spravato or antidepressants have been run; while not indicated for TRD, traditional antidepressants are frequently used to treat TRD patients as there are limited treatment options currently indicated for this patient population

31 | © Compass Pathways Clinical care teams KOLs/HCPs Federal and State policy makers Patient advocacy organizations Payers DEA rescheduling (Federal & State) Product distribution Pricing & Reimbursement Formulary access Patient Support Commercial team build-out Product positioning Site of care training Field force strategy Omni-channel marketing We are Planning To Be Launch Ready by the End of the Year NOTE: KOL = key opinion leaders; HCP = healthcare professional Enable Awareness & Access Enable Patient AccessLaunch ReadinessEducate & Learn

32 | © Compass Pathways Summary • The emerging clinical profile of COMP360 is redefining rapidity and durability for TRD patients • TRD is a chronic and extremely refractory condition with very few treatment options - No approved drug offers clinically meaningful efficacy with both rapid onset and sustained durability with a single treatment • The robust benefit/risk profile of COMP360 supports a potentially highly compelling, novel paradigm for patients and providers where effectiveness may be determined almost immediately after a single treatment - Patients with a clinically meaningful reduction in MADRS from the first treatment have shown the potential for sustained benefit through at least 26 weeks, after one or two doses • These results increase our conviction in the potential importance of this treatment for TRD patients • We are planning to meet as soon as possible with the FDA to discuss a rolling submission and review, and expect to complete an NDA submission in Q4 • COMP360 has Breakthrough Therapy designation from the FDA

33 | © Compass Pathways Thank you… Q&A For more information: Stephen Schultz SVP, Investor Relations stephen.schultz@compasspathways.com +1 401-290-7324

35 | © Compass Pathways MedDRA = Medical Dictionary for Regulatory Activities; N=number of participants in the treatment group in the Safety Analysis Set by administration; n = number of participants. Note: COMP006 safety includes 2 dose administrations and goes out to 9 weeks vs. 1 administration out to 6 weeks for COMP005 COMP006 - Treatment-Emergent Adverse Events (TEAE) – Incidence >5% COMP360 1 mg COMP360 10 mg COMP360 25 mg COMP006 (>5% Incidence) MedDRA EAE Preferred Term N=143N=142N=296 n (%)n (%) n (%) 80 (55.9)111 (78.2)254 (85.8)Any TEAE 15 (10.5)42 (29.6)118 (39.9)Nausea 41 (28.7)43 (30.3)108 (36.5)Headache 21 (14.7)28 (19.7)62 (20.9)Anxiety 3 (2.1)24 (16.9)46 (15.5)Hallucination, visual 3 (2.1)16 (11.3)41 (13.9)Illusion 9 (6.3)21 (14.8)41 (13.9)Dizziness 16 (11.2)23 (16.2)41 (13.9)Fatigue 4 (2.8)13 (9.2)35 (11.8)Crying 4 (2.8)6 (4.2)31 (10.5)Blood pressure increased 10 (7.0)15 (10.6)19 (6.4)Insomnia 3 (2.1)6 (4.2)17 (5.7)Tearfulness 02 (1.4)15 (5.1)Vomiting 6 (4.2)9 (6.3)15 (5.1)Back pain 2 (1.4)8 (5.6)14 (4.7)Mood altered 3 (2.1)10 (7.0)13 (4.4)Feeling cold 5 (3.5)8 (5.6)10 (3.4)Major depression 9 (6.3)7 (4.9)8 (2.7)Suicidal ideation 08 (5.6)7 (2.4)Hallucination, auditory

Source: View Original Filing on SEC EDGAR

FAQ

What did Compass Pathways (CMPS) announce about its COMP360 Phase 3 trials?

Compass Pathways reported that both pivotal Phase 3 trials of COMP360 in treatment-resistant depression met their primary endpoints, showing statistically significant MADRS score improvements versus control arms at Week 6, with rapid onset from the day after dosing and meaningful durability in responders.

How effective was COMP360 in reducing depression symptoms in the COMP005 and COMP006 studies?

In COMP005, a single 25 mg COMP360 dose produced a -3.6 point MADRS difference versus placebo at Week 6. In COMP006, two 25 mg doses gave a -3.8 point difference versus 1 mg at Week 6, with 39% of 25 mg patients achieving at least a 25% MADRS reduction.

What safety profile did COMP360 show in Compass Pathways’ Phase 3 TRD program?

Across COMP005 and COMP006, COMP360 was generally well-tolerated. Most treatment-emergent adverse events, such as headache, nausea, anxiety and visual hallucinations, occurred on dosing days and resolved within a day, while serious suicidal events were rare across all treatment arms.

How durable were COMP360’s treatment effects in treatment-resistant depression patients?

In COMP005, 25% of patients on 25 mg achieved a clinically meaningful MADRS reduction at Week 6 and maintained benefit through at least Week 26 after one or two doses, indicating potentially durable symptom relief in a subset of treatment-resistant depression patients.

What regulatory steps is Compass Pathways (CMPS) planning after these Phase 3 results?

Compass Pathways plans to meet with the U.S. FDA to discuss a rolling NDA submission and review for COMP360 in treatment-resistant depression, and currently expects to complete an NDA submission in Q4, supported by COMP360’s Breakthrough Therapy designation.

How large were the COMP005 and COMP006 Phase 3 trials for COMP360 in TRD?

The COMP005 single-dose Phase 3 trial included 258 dosed participants, with 171 on COMP360 25 mg and 87 on placebo. The COMP006 multiple-dose trial enrolled 581 participants, including 296 on 25 mg, 142 on 10 mg and 143 on 1 mg COMP360.

Filing Exhibits & Attachments

4 documents

Press Releases

EX-99.1 EX-99.1 45.8 KB

Compass Pathways (NASDAQ: CMPS) reports strong positive Phase 3 TRD results