Definium Therapeutics (DFTX) offers $500M in shares and pre-funded warrants
Definium Therapeutics, Inc. is offering $500,000,000 of common shares and pre-funded warrants pursuant to a preliminary prospectus supplement dated June 22, 2026 (subject to completion). The shares trade on Nasdaq under DFTX; the last reported sale price on June 18, 2026 was $24.48 per share.
The prospectus supplement relates to a primary shelf offering of common shares and pre-funded warrants, and discloses pro forma share counts including 104,044,508 common shares outstanding as of March 31, 2026. The offering includes a 30-day underwriter option to purchase up to an additional $75,000,000 of common shares. The supplement also summarizes recent clinical developments: the Phase 3 Emerge study in MDD met its primary and key secondary endpoints (MADRS LS mean change at Week 6: -13.3 for DT120 100 µg vs -5.2 for placebo; placebo-adjusted difference -8.1, p<0.0001).
Positive
- Emerge (DT120) met primary and key secondary endpoints in MDD: MADRS LS mean change Week 6 -13.3 vs placebo -5.2 (placebo-adjusted -8.1, p<0.0001)
Negative
- None.
Insights
Offering is a primary shelf sale with an up to $75M option; standard structure and investor protections.
The supplement documents a primary offering of common shares and pre-funded warrants under an S-3 shelf; it discloses an underwriter overallotment option of $75,000,000 and customary exercise limits on the pre-funded warrants (beneficial ownership caps at 4.99%/9.99% initial elections).
Subscription mechanics, exercise-price adjustment clauses, and transferability are described; the pre-funded warrants are not expected to be listed and carry customary liquidity limitations. Cash-flow treatment on exercise is stated as nominal; proceeds estimates are provided but specific per-share offering price fields are redacted in the excerpt.
Clinical readouts anchor the filing: Emerge showed a robust MADRS treatment effect; Phase 3 GAD program enrollment and timing are disclosed.
The Emerge topline showed an LS mean change in MADRS at Week 6 of -13.3 for DT120 100 µg versus -5.2 for placebo (placebo-adjusted difference -8.1, p<0.0001). Safety outcomes reported were generally consistent with expected acute effects.
Phase 3 GAD trials (Voyage enrolled 214; Panorama enrolled 245 with a target update to 200 after SSRE) are on near-term readout timelines: Voyage Part A expected early Q3 2026 and Panorama Part A expected late Q3 2026. Subsequent regulatory and commercial milestones remain conditional on full data and approvals.
Key Figures
Key Terms
pre-funded warrant financial
blinded interim sample size re-estimation (SSRE) clinical
MADRS clinical
ODT (orally disintegrating tablet) clinical
Offering Details
(to Prospectus dated June 28, 2024)
| | | |
Per share
|
| |
Per pre-funded
warrant |
| |
Total
|
| |||||||||
| Public Offering Price | | | | $ | | | | | $ | | | | | $ | | | |||
| Underwriting Discounts and Commissions(1) | | | | $ | | | | | | $ | | | | | | $ | | | |
| Proceeds to Definium Therapeutics, Inc. before expenses | | | | $ | | | | | | $ | | | | | | $ | | | |
| | J.P. Morgan | | |
Jefferies
|
| |
Leerink Partners
|
| |
BofA Securities
|
|
| |
Evercore ISI
|
| |
Stifel
|
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Oppenheimer & Co.
|
| |
LifeSci Capital
|
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ABOUT THIS PROSPECTUS SUPPLEMENT
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| | | | S-ii | | |
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PROSPECTUS SUPPLEMENT SUMMARY
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| | | | S-1 | | |
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THE OFFERING
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| | | | S-7 | | |
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RISK FACTORS
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| | | | S-10 | | |
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SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
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| | | | S-13 | | |
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USE OF PROCEEDS
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| | | | S-16 | | |
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DIVIDEND POLICY
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| | | | S-17 | | |
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DILUTION
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| | | | S-18 | | |
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DESCRIPTION OF THE SECURITIES WE ARE OFFERING
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| | | | S-20 | | |
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CERTAIN CANADIAN FEDERAL INCOME TAX CONSIDERATIONS
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| | | | S-23 | | |
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CERTAIN U.S. FEDERAL INCOME TAX CONSIDERATIONS
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| | | | S-25 | | |
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UNDERWRITING
|
| | | | S-33 | | |
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LEGAL MATTERS
|
| | | | S-39 | | |
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EXPERTS
|
| | | | S-39 | | |
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WHERE YOU CAN FIND MORE INFORMATION
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| | | | S-39 | | |
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INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
|
| | | | S-40 | | |
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ENFORCEABILITY OF CIVIL LIABILITIES
|
| | | | S-41 | | |
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ABOUT THIS PROSPECTUS
|
| | | | ii | | |
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SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
|
| | | | 1 | | |
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MARKET, INDUSTRY AND OTHER DATA
|
| | | | 3 | | |
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THE COMPANY
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| | | | 4 | | |
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RISK FACTORS
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| | | | 8 | | |
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USE OF PROCEEDS
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| | | | 9 | | |
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SELLING SECURITYHOLDERS
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| | | | 10 | | |
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PLAN OF DISTRIBUTION
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| | | | 11 | | |
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GENERAL DESCRIPTION OF OUR SECURITIES
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| | | | 14 | | |
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DESCRIPTION OF OUR COMMON SHARES
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| | | | 15 | | |
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DESCRIPTION OF OUR WARRANTS
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| | | | 16 | | |
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DESCRIPTION OF OUR DEBT SECURITIES
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| | | | 18 | | |
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DESCRIPTION OF OUR UNITS
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| | | | 23 | | |
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WHERE YOU CAN FIND MORE INFORMATION
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| | | | 24 | | |
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INCORPORATION BY REFERENCE
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| | | | 24 | | |
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LEGAL MATTERS
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| | | | 24 | | |
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EXPERTS
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| | | | 25 | | |
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Endpoint
|
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DT120 ODT
100 µg |
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Placebo ODT
|
| | |
Placebo-Adjusted
Difference |
| |
| | | MADRS: LS mean change at Week 6* | | | |
-13.3
|
| | |
-5.2
|
| | |
-8.1 (p<0.0001)
|
| |
| | | MADRS: LS mean change at Week 12** | | | |
-11.0
|
| | |
-3.6
|
| | |
-7.3 (p<0.0001)
|
| |
| | | MADRS: LS mean change at Week 1** | | | |
-17.6
|
| | |
-3.4
|
| | |
-14.2 (p<0.0001)
|
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| | | CGI-S: LS mean change at Week 6** | | | |
-1.2
|
| | |
-0.3
|
| | |
-0.9 (p<0.0001)
|
| |
| | |
Endpoint
|
| | |
DT120 ODT
100 µg |
| | |
Placebo ODT
|
| | |
Placebo-Adjusted
Difference |
| |
| | | CGI-S: LS mean change at Week 12** | | | |
-1.0
|
| | |
-0.3
|
| | |
-0.7 (p<0.0001)
|
| |
| | | CGI-S: LS mean change at Day 2** | | | |
-1.0
|
| | |
-0.1
|
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-0.9 (p<0.0001)
|
| |
| | | MADRS: response rate (≥50%) at Week 6*** | | | |
35%
|
| | |
7%
|
| | |
28% (p<0.001)
|
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| | | MADRS: remission rate (≤12) at Week 6*** | | | |
24%
|
| | |
3%
|
| | |
21% (p<0.01)
|
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| |
Public offering price per common share
|
| | | | | | | | | $ | | | |
| |
Net tangible book value per common share as of March 31, 2026
|
| | | $ | 2.49 | | | | | | | | |
| |
Increase per common share attributable to sale of common shares in this offering
|
| | | | | | | | | | | | |
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As adjusted net tangible book value per common share after this offering
|
| | | | | | | | | | | | |
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Dilution per common share to new investors in this offering
|
| | | | | | | | | $ | | | |
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Name
|
| |
Number of
common shares |
| |
Number of
pre-funded warrants |
|
|
J.P. Morgan Securities LLC
|
| | | | | | |
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Jefferies LLC
|
| | | ||||
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Leerink Partners LLC
|
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BofA Securities, Inc.
|
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Evercore Group L.L.C.
|
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Stifel, Nicolaus & Company, Incorporated
|
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Oppenheimer & Co. Inc.
|
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LifeSci Capital LLC
|
| | | | | | |
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Total
|
| | | | | | |
| | | |
Without
option to purchase additional common shares exercise |
| |
With full
option to purchase additional common shares exercise |
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|
Per Common Share
|
| | | $ | | | | | $ | | | ||
|
Per Pre-Funded Warrant
|
| | | $ | | | | | $ | | | ||
|
Total
|
| | | $ | | | | | $ | | | | |
Attention: Corporate Secretary
One World Trade Center, Suite 8500,
New York, New York 10007
Telephone: (212) 220-6633
Warrants
Debt Securities
Units
| |
ABOUT THIS PROSPECTUS
|
| | | | ii | | |
| |
SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
|
| | | | 1 | | |
| |
MARKET, INDUSTRY AND OTHER DATA
|
| | | | 3 | | |
| |
THE COMPANY
|
| | | | 4 | | |
| |
RISK FACTORS
|
| | | | 8 | | |
| |
USE OF PROCEEDS
|
| | | | 9 | | |
| |
SELLING SECURITYHOLDERS
|
| | | | 10 | | |
| |
PLAN OF DISTRIBUTION
|
| | | | 11 | | |
| |
GENERAL DESCRIPTION OF OUR SECURITIES
|
| | | | 14 | | |
| |
DESCRIPTION OF OUR COMMON SHARES
|
| | | | 15 | | |
| |
DESCRIPTION OF OUR WARRANTS
|
| | | | 16 | | |
| |
DESCRIPTION OF OUR DEBT SECURITIES
|
| | | | 18 | | |
| |
DESCRIPTION OF OUR UNITS
|
| | | | 23 | | |
| |
WHERE YOU CAN FIND MORE INFORMATION
|
| | | | 24 | | |
| |
INCORPORATION BY REFERENCE
|
| | | | 24 | | |
| |
LEGAL MATTERS
|
| | | | 24 | | |
| |
EXPERTS
|
| | | | 25 | | |
| | J.P. Morgan | | |
Jefferies
|
| |
Leerink Partners
|
| |
BofA Securities
|
|
| |
Evercore ISI
|
| |
Stifel
|
| ||||||
| |
Oppenheimer & Co.
|
| |
LifeSci Capital
|
| ||||||