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InMed Pharmaceuticals & Mentari Therapeutics Announce Merger to Advance Migraine Prevention Therapies

Rhea-AI Impact
(High)
Rhea-AI Sentiment
(Positive)

InMed (NASDAQ:INM) agreed to an all-stock merger with privately held Mentari Therapeutics, creating a Nasdaq-listed company focused on migraine prevention.

A concurrent oversubscribed US$290 million private placement is expected to fund operations through 2028, supporting development of lead antibodies MT-001 and MT-002 with key clinical readouts targeted for 2027–2028.

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AI-generated analysis. Not financial advice.

Positive

  • US$290 million private placement expected to fund operations through 2028
  • All-stock merger gives Mentari access to public market infrastructure
  • Lead programs MT-001 and MT-002 have defined clinical timelines
  • MT-002 positioned as anti-CGRP and anti-PACAP bispecific antibody

Negative

  • MT-001 Phase 2a proof-of-concept data not expected until 2028
  • MT-002 first-in-human Phase 1 data only expected in 2027

Key Figures

Private placement size: US$290 million First-in-human MT-001: mid-2026 First-in-human MT-002: 1Q 2027 +5 more
8 metrics
Private placement size US$290 million Concurrent oversubscribed private placement to fund operations through 2028
First-in-human MT-001 mid-2026 Expected timing for first-in-human regulatory filings for MT-001
First-in-human MT-002 1Q 2027 Expected timing for first-in-human regulatory filings for MT-002
MT-001 Phase 2a data 2028 Expected timing for Phase 2a proof-of-concept data in migraine prevention
MT-002 Phase 1 data 2027 Expected timing for Phase 1 healthy volunteer data
Global migraine population more than 1 billion people Estimated worldwide population affected by migraine
Suboptimal 50% MMD response approximately 40-50% of patients Patients on current therapies not achieving 50% reduction in MMDs
High 75% MMD response fewer than one-third of patients Patients achieving 75% reduction in monthly migraine days

Market Reality Check

Price: $0.6807 Vol: Volume 10,242 is below 20...
low vol
$0.6807 Last Close
Volume Volume 10,242 is below 20-day average of 23,229 (relative volume 0.44x). low
Technical Price 0.6807 is trading below the 200-day MA at 1.40 and far under the $7.98 52-week high.

Peers on Argus

INM is up 6.34% while 4 momentum-screened peers (e.g., SBFM, CPHI) are all down ...
4 Down

INM is up 6.34% while 4 momentum-screened peers (e.g., SBFM, CPHI) are all down (median move about -8.3%), signaling stock-specific strength against sector weakness.

Historical Context

5 past events · Latest: May 06 (Negative)
Pattern 5 events
Date Event Sentiment Move Catalyst
May 06 Earnings and update Negative -4.1% Q3 2026 loss, cash position and BayMedica wind-down details.
Apr 27 Option repricing Negative -4.3% Lowered exercise prices on preferred investment options.
Mar 27 Nasdaq notice Negative -6.2% Noncompliance with Nasdaq minimum $1.00 bid requirement.
Mar 23 Preclinical data Positive -6.9% Positive INM-901 human brain organoid neuroinflammation results.
Mar 09 Pipeline update Positive -3.7% Development roadmap for INM-901 and INM-089 toward IND filings.
Pattern Detected

Across the last five news events, INM’s shares traded lower after both positive R&D updates and negative regulatory/financial developments, with three aligned selloffs on negative items and two divergences where positive news also saw declines.

Recent Company History

Over the last several months, INM focused on CNS drug development while managing financial and listing pressures. Updates on INM-901 and other candidates in March–May 2026 highlighted preclinical neuroinflammation data and IND-planning steps, yet each event saw share-price declines. The company also faced a Nasdaq minimum bid-price notice and amended investment options at lower exercise prices. Against this backdrop, the Mentari merger and large migraine-focused pipeline represent a strategic shift from earlier INM-901–centric communications and BayMedica wind-down disclosures.

Regulatory & Risk Context

Active S-3 Shelf · $50,000,000
Shelf Active
Active S-3 Shelf Registration 2026-03-20
$50,000,000 registered capacity

InMed has an effective Form S-3 shelf filed on 2026-03-20, allowing offerings of up to $50,000,000 in various securities. The company has already used this shelf via a 424B5 filed on 2026-04-03 for an at-the-market offering of up to $1,213,648 of common shares, providing flexibility for future capital raises alongside the announced Mentari financing.

Market Pulse Summary

This announcement combines an all-stock merger bringing in Mentari’s migraine-prevention pipeline wi...
Analysis

This announcement combines an all-stock merger bringing in Mentari’s migraine-prevention pipeline with a concurrent US$290 million private placement expected to fund operations through 2028. It marks a strategic shift from prior INM updates focused on INM-901 and BayMedica’s wind-down. Investors may track execution on MT-001 and MT-002 timelines, integration progress, and the use of existing capital-raising tools under the $50,000,000 S-3 shelf and ATM prospectus, alongside Nasdaq listing compliance developments.

Key Terms

anti-cgrp, monoclonal antibody, bispecific antibody, subcutaneous delivery, +2 more
6 terms
anti-cgrp medical
"Mentari's parallel lead programs target validated, complementary pathways with potential..."
A class of medicines that block calcitonin gene-related peptide (CGRP) or its receptor—a chemical messenger that helps trigger migraine pain and blood-vessel changes. Think of them as turning down the volume on a specific pain signal rather than treating all symptoms; they can prevent or reduce migraine attacks. Investors watch anti-CGRP drugs because migraines affect many people, creating steady demand, and because pricing, approval status, and competition determine revenue and long-term returns.
monoclonal antibody medical
"MT-001, an anti-PACAP ... monoclonal antibody with Phase 2a proof-of-concept data expected..."
A monoclonal antibody is a laboratory-made protein designed to recognize and attach to a specific target in the body, such as a disease-causing substance or cell. It functions like a highly precise lock-and-key tool, helping to treat or detect illnesses. For investors, companies developing monoclonal antibodies can represent promising opportunities in the healthcare sector, especially as these treatments often address unmet medical needs.
bispecific antibody medical
"MT-002, a potentially first-in-class anti-CGRP and anti-PACAP bispecific antibody..."
A bispecific antibody is a specially designed protein that can attach to two different targets at the same time. Think of it as a custom-made connector that brings two things together—such as a disease cell and an immune system component—helping the body fight illnesses more effectively. For investors, understanding bispecific antibodies is important because they represent innovative therapies that could lead to new treatments and potentially lucrative market opportunities.
subcutaneous delivery medical
"designed to be potentially best-in-class, with superior convenience through subcutaneous delivery..."
Subcutaneous delivery is a method of giving a drug or vaccine by injecting it just under the skin into the layer of tissue between the skin and muscle, similar to tucking a tiny package under a shirt rather than sewing it into a coat. It matters to investors because this route can make treatments easier to administer outside hospitals, reduce costs, improve patient convenience and adherence, and therefore affect a product’s commercial success and pricing.
phase 2a medical
"monoclonal antibody with Phase 2a proof-of-concept data expected in 2028..."
Phase 2a is an early stage in testing a new medical treatment or drug, where the main goal is to assess its safety and find the right dosage. For investors, this stage indicates whether the treatment shows initial promise before moving on to larger, more definitive studies; progress here can influence expectations for future development and potential success.
phase 1 medical
"bispecific antibody with Phase 1 healthy volunteer data expected in 2027."
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.

AI-generated analysis. Not financial advice.

Mentari's parallel lead programs target validated, complementary pathways with potential to address the two-thirds of patients who have a suboptimal response to anti-CGRP therapies

Concurrent oversubscribed US$290 million private placement of Mentari expected to fund company operations through 2028

First-in-human regulatory filings for MT-001 (anti-PACAP) and MT-002 (anti-CGRP x PACAP bispecific) expected mid-2026 and 1Q 2027, respectively

Conference call scheduled for May 19, 2026, at 8:30 AM EDT

VANCOUVER, BC and SAN FRANCISCO, May 19, 2026 /PRNewswire/ -- InMed Pharmaceuticals, Inc. (NASDAQ: INM) ("InMed" or the "Company") is pleased to announce that it has entered into a definitive merger agreement (the "Agreement") for an all-stock transaction with Mentari Therapeutics, Inc. ("Mentari"), a privately-held biotechnology company developing therapies for migraine prevention, Indigo Merger Sub Corp. a wholly-owned subsidiary of InMed, and Indigo Merger Sub II, LLC, a wholly-owned subsidiary of InMed. The merger brings together Mentari's differentiated migraine pipeline with InMed's public market infrastructure, positioning the combined company to expedite the development of new therapies for people living with migraine, a debilitating neurological disorder affecting more than 1 billion people globally. Upon consummation of the transaction contemplated by the Agreement, the combined entity will operate as Mentari Therapeutics and trade on the Nasdaq Capital Market under a new ticker symbol.

The concurrent private placement (the "Private Placement") was led by Fairmount with participation from Commodore Capital, Deep Track Capital, Janus Henderson Investors, a16z Bio + Health, Venrock Healthcare Capital Partners, Wellington Management, TCGX, Blackstone Multi-Asset Investing, BB Biotech, Farallon Capital, RTW Investments, LP, Vivo Capital, Perceptive Advisors and other leading investment management firms. The Private Placement will result in gross proceeds to the combined company of approximately US$290 million and is expected to fully fund its operations through 2028, beyond the generation of anticipated key clinical datasets from Mentari's parallel lead programs. These programs include MT-001, an anti-PACAP (pituitary adenylate cyclase-activating polypeptide) monoclonal antibody with Phase 2a proof-of-concept data expected in 2028, and MT-002, a potentially first-in-class anti-CGRP (calcitonin gene-related peptide) and anti-PACAP bispecific antibody with Phase 1 healthy volunteer data expected in 2027. Together, MT-001 and MT-002 target validated, complementary, and orthogonal pathways in migraine pathophysiology and have potential to address the significant unmet need in individuals suffering from chronic and episodic migraine. Approximately 40-50% of patients treated with current approved therapies do not achieve a 50% reduction in monthly migraine days (MMDs), and fewer than one-third of patients have a 75% reduction in MMDs.

"This merger with Mentari represents an excellent opportunity for InMed shareholders to participate in the development of an exciting new drug pipeline with significant therapeutic and commercial potential," said Eric A. Adams, President and CEO of InMed. "InMed's Board of Directors and management team are in full support of this transaction and believe that Mentari's strong balance sheet positions the company to successfully execute on the development plans for its parallel lead programs in the treatment of migraines. We believe Mentari's lead programs have tremendous potential to expand and reshape the migraine treatment and prevention market."

"This transaction provides us with the capital and public market infrastructure to aggressively compete in what we believe will be the next era of migraine prevention," said Julie Bruno, Chair of Mentari's board. "Recent anti-PACAP clinical studies have validated this novel mechanism and generated tremendous excitement among headache specialists. MT-001 and MT-002 were designed to be potentially best-in-class, with superior convenience through subcutaneous delivery and the potential for enhanced efficacy through rational dual pathway inhibition. We have a clear regulatory path, rapid development timelines benchmarked to approved migraine therapies, and are focused on bringing these potentially transformative therapies to the millions of people who continue to suffer despite current treatment options."

Mentari's pipeline programs were discovered by Paragon Therapeutics, Inc. and the co-lead programs, MT-001 and MT-002, have demonstrated equal or superior in vitro potency compared to benchmark antibodies, with pharmacokinetic profiles in non-human primates projected to enable convenient subcutaneous dosing in humans.

Conference Call Details

InMed will host a conference call on Tuesday, May 19th, at 8:30 am ET to discuss the merger details. To join the call, please dial (888) 880-3330 (U.S Toll Free) or (800) 715-9871 (Canada Toll Free). A replay of the call will be temporarily archived on the Investors section of InMed's website following the presentation.

About the Proposed Transaction

Under the terms of the merger agreement, as of the closing of the proposed merger, the pre-merger InMed shareholders are expected to own approximately 1.51% of the combined company, which is expected to have a pro forma equity value of approximately US$421.4 million (inclusive of the Private Placement). The percentage of the combined company that InMed's shareholders will own as of the closing of the proposed merger is subject to adjustment based on the estimated amount of InMed's net cash immediately prior to the closing date.

In addition, InMed shareholders as of immediately prior to Closing (the "Holders") will be entitled to receive additional financial consideration through (i) a potential distribution or dividend (if any) (1) payable upon a pre-closing sale, license, divestiture or other monetization transaction (i.e., a royalty transaction) of InMed research and development programs (a "Parent Legacy Transaction"), and (2) to the extent closing net cash exceeds certain thresholds described in the Agreement; and (ii) a contingent value right entitling the Holders to proceeds (if any) from a Parent Legacy Transaction received post-closing, in each case the terms of which will be described in the Agreement and/or Form 8-K to be filed in connection with the proposed transaction.

The transaction has received approval by the Board of Directors of both companies and is expected to close in the second half of 2026, subject to certain closing conditions, including, among others, approval by the stockholders of each company, the effectiveness of a registration statement to be filed with the U.S. Securities and Exchange Commission (the "SEC") to register the securities to be issued in connection with the proposed merger and the satisfaction of other customary closing conditions.

The combined company plans to operate under the name Mentari Therapeutics, Inc. Mentari's existing Board of Directors will become directors of the combined company, chaired by Julie Bruno, Growth Partner at Fairmount, and including Michelle Pernice, Operating Partner at Fairmount, and Laura Sandler, Chief Operating Officer at Oruka Therapeutics.

Lucid Capital Markets, LLC is serving as financial advisor and Norton Rose Fulbright LLP and Norton Rose Fulbright Canada LLP are serving as legal counsel to InMed. Wedbush Securities Inc. is serving as exclusive strategic financial advisor and Gibson, Dunn & Crutcher LLP is serving as legal counsel to Mentari. Jefferies, TD Cowen, Stifel, UBS Investment Bank, and Wedbush & Co., LLC are serving as the placement agents to Mentari. Cooley LLP is serving as legal counsel to the placement agents.

About InMed Pharmaceuticals

InMed is a pharmaceutical company focused on developing a pipeline of proprietary small molecule drug candidates targeting the CB1/CB2 receptors. InMed's pipeline consists of three separate programs in the treatment of Alzheimer's, ocular and dermatological indications. For more information, visit www.inmedpharma.com.

About Mentari Therapeutics

Mentari Therapeutics is a biotechnology company developing therapies for the prevention of migraine to deliver freedom from this debilitating and undertreated neurological condition that affects more than 1 billion people globally. Mentari's lead programs target PACAP, a newly validated target that is mechanistically independent from CGRP, one of the first migraine targets to yield clinical and commercial success. Mentari's pipeline includes MT-001, an anti-PACAP monoclonal antibody designed for convenient subcutaneous dosing, and MT-002, an anti-CGRP and anti-PACAP bispecific antibody designed to inhibit these complementary pathways with potential to deliver superior outcomes for people with incomplete response to CGRP-targeted therapies. The company's programs were discovered by Paragon Therapeutics. Mentari is based in Waltham, MA. For more information, visit mentaritx.com.

Forward Looking Statements

Certain statements in this press release, other than purely historical information, may constitute "forward-looking statements" within the meaning of the federal securities laws, including for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements relating to InMed's and Mentari's expectations, hopes, beliefs, intentions or strategies regarding the proposed merger, the Private Placement, and the combined company's future, pipeline and business including, without limitation, statements regarding the expected timing and completion of the proposed merger and the Private Placement, the anticipated ownership structure of the combined company, the expected benefits, opportunities and market potential of the proposed transaction, the combined company's ability to achieve the expected benefits or opportunities with respect to its product candidates, including whether MT-001 and MT-002 will achieve clinical proof of concept, demonstrate superior efficacy or potency, achieve convenient dosing, address unmet need in CGRP inadequate responders, or achieve regulatory approval and statements made herein with respect to (i) a potential distribution or dividend (if any) (A) payable upon a Parent Legacy Transaction, and (B) to the extent closing net cash exceeds certain thresholds described in the Agreement, and (ii) the contingent value rights entitling the Holders to proceeds (if any) from a Parent Legacy Transaction received post-closing. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. These forward-looking statements are based on current expectations and beliefs concerning future developments and their potential effects. There can be no assurance that future developments affecting the combined company will be those that have been anticipated. These forward-looking statements involve a number of risks, uncertainties (some of which are beyond InMed's, Mentari's or the combined company's control) or other assumptions that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to, risks related to: the risk that the proposed merger and the Private Placement may not be completed on the anticipated timeline or at all; the failure to satisfy the conditions to closing, including obtaining the requisite approvals of the stockholders of each company and the effectiveness of the registration statement to be filed with the SEC in connection with the proposed merger; the risk that the Private Placement may not close or may not result in the anticipated gross proceeds; the outcome of preclinical studies and clinical trials; regulatory approval processes; the combined company's ability to successfully develop and commercialize its product candidates; competition in the migraine treatment market; the combined company's reliance on third parties; protection of intellectual property; and the combined company's need for substantial additional funding. Should one or more of these risks or uncertainties materialize, or should any of InMed's, Mentari's or the combined company's assumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth therein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements in this press release, which speak only as of the date they are made and are qualified in their entirety by reference to the cautionary statements herein and in InMed's filings with the SEC. InMed, Mentari and the combined company do not undertake or accept any duty to make any updates or revisions to any forward-looking statements, except as required by law.

Important Information About Investigational Product Candidates

This press release concerns drug candidates that are under preclinical and clinical investigation, and which have not yet been approved by the U.S. Food and Drug Administration. These are currently limited by federal law to investigational use, and no representation is made as to their safety or effectiveness for the purposes for which they are being investigated.

No Offer or Solicitation

This press release is not intended to and does not constitute an offer to sell or the solicitation of an offer to buy any securities, or a solicitation of any proxy, vote, consent or approval, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. The securities to be sold in the Private Placement are being offered in a transaction not involving a public offering and have not been registered under the Securities Act of 1933, as amended, or any state securities laws, and may not be offered or sold in the United States absent registration or an applicable exemption from the registration requirements.

NEITHER THE SEC NOR ANY STATE SECURITIES COMMISSION HAS APPROVED OR DISAPPROVED OF THE SECURITIES OR DETERMINED IF THIS COMMUNICATION IS TRUTHFUL OR COMPLETE.

Important Additional Information About the Proposed Transaction Will Be Filed with the SEC

In connection with the proposed merger, InMed intends to file relevant materials with the SEC, including a registration statement on Form S-4 that will contain a proxy statement/prospectus relating to the proposed transaction. This press release is not a substitute for the registration statement, proxy statement/prospectus or any other document that InMed may file with the SEC in connection with the proposed transaction.

INVESTORS AND SECURITY HOLDERS OF INMED AND MENTARI ARE URGED TO READ THE REGISTRATION STATEMENT, PROXY STATEMENT/PROSPECTUS AND ANY OTHER RELEVANT DOCUMENTS FILED OR TO BE FILED WITH THE SEC, AS WELL AS ANY AMENDMENTS OR SUPPLEMENTS THERETO, CAREFULLY AND IN THEIR ENTIRETY IF AND WHEN THEY BECOME AVAILABLE, BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT INMED, MENTARI, THE PROPOSED TRANSACTION AND RELATED MATTERS.

Investors and security holders will be able to obtain free copies of the registration statement, proxy statement/prospectus and other documents filed by InMed with the SEC through the website maintained by the SEC at www.sec.gov and on the Investors section of InMed's website.

Participants in the Solicitation

InMed, Mentari and their respective directors and executive officers may be deemed to be participants in the solicitation of proxies from InMed's stockholders in connection with the proposed transaction. Information about InMed's directors and executive officers, including a description of their interests in InMed, is contained in InMed's most recent Annual Report on Form 10-K and subsequent reports filed with the SEC. Additional information regarding the persons who may, under the rules of the SEC, be deemed participants in the solicitation of proxies in connection with the proposed transaction, including a description of their direct or indirect interests, by security holdings or otherwise, will be included in the registration statement and proxy statement/prospectus when filed with the SEC.

Media Contact

Lia Dangelico
Deerfield Group
lia.dangelico@deerfieldgroup.com

Investor Contact
Colin Clancy
Vice President, Investor Relations
and Corporate Communications, InMed Pharmaceuticals Inc.
T:  +1.604.416.0999
E:   ir@inmedpharma.com

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/inmed-pharmaceuticals--mentari-therapeutics-announce-merger-to-advance-migraine-prevention-therapies-302776112.html

SOURCE InMed Pharmaceuticals

FAQ

What did InMed (NASDAQ:INM) announce about its merger with Mentari Therapeutics on May 19, 2026?

InMed announced an all-stock merger with Mentari Therapeutics to create a Nasdaq-listed migraine-focused company. According to InMed, the combined entity will operate as Mentari Therapeutics and concentrate on preventive antibody therapies MT-001 and MT-002 for chronic and episodic migraine patients.

How much is the Mentari Therapeutics private placement tied to the InMed (INM) merger?

The associated private placement is expected to raise approximately US$290 million in gross proceeds. According to InMed, this oversubscribed financing should fully fund the combined company’s operations through 2028, including planned clinical development of migraine prevention candidates MT-001 and MT-002.

When are key clinical milestones for Mentari’s MT-001 and MT-002 after the InMed (INM) merger?

First-in-human filings for MT-001 are targeted for mid-2026, with Phase 2a data in 2028. According to InMed, MT-002’s first-in-human filing is expected in Q1 2027, with Phase 1 healthy volunteer data anticipated later in 2027.

What migraine pathways do Mentari’s MT-001 and MT-002 target following the InMed (INM) merger?

MT-001 targets PACAP, while MT-002 targets both CGRP and PACAP pathways. According to Mentari, these validated, complementary and orthogonal mechanisms may help address patients who have suboptimal response to current anti-CGRP migraine prevention therapies.

How might the InMed and Mentari merger impact funding runway for the combined company?

The US$290 million private placement is expected to fund operations through 2028. According to InMed, this runway extends beyond anticipated key clinical datasets from MT-001 and MT-002, supporting parallel development of both migraine prevention programs.

When is the InMed (INM) conference call to discuss the Mentari merger?

The conference call is scheduled for May 19, 2026, at 8:30 AM ET. According to InMed, investors can join via U.S. and Canada toll-free numbers, with a replay temporarily available in the Investors section of the company’s website.