Earnings release
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August 6 , 2026 Definium >> THERAPEUTICS Definium Therapeutics Reports Second Quarter 2026 Financial Results and Recent Highlights Announced positive topline results from Phase 3 Emerge study of DT120 ODT in major depressive disorder ( MDD ) , demonstrating rapid , robust , and durable efficacy Topline results from Phase 3 GAD studies of DT120 ODT in generalized anxiety disorder ( GAD ) on track : Voyage results anticipated week of August 10 ; Panorama results anticipated September 2026 Approximately $ 1.1 billion in cash , cash equivalents , and investments as of June 30 , 2026 Conference call scheduled today at 4:30 p.m. EDT NEW YORK -- ( BUSINESS WIRE ) -- Definium Therapeutics , Inc. ( " Definium ” or the " Company " ) ( NASDAQ : DFTX ) , a late - stage clinical biopharmaceutical company developing a new generation of therapeutics intended to address underlying causes of psychiatric and neurological disorders , today reported financial results for the quarter ended June 30 , 2026 , and recent highlights . " The second quarter marked a meaningful inflection point for Definium as we further established our leadership position in psychedelic medicine , ” said Rob Barrow , Chief Executive Officer of Definium Therapeutics . “ The unprecedented Phase 3 Emerge results validated the highly differentiated profile of DT120 ODT and reinforced its potential to become a best - in - class treatment across multiple psychiatric disorders . We also continued to execute across our pipeline , completing enrollment in Voyage and Panorama and initiating enrollment in Ascend . Our public offering generated approximately $ 805 million in gross proceeds and provides the capital to advance our clinical and commercial strategy from a position of strength . We believe Definium is uniquely positioned to advance a potential new treatment paradigm across some of the field's largest and most underserved indications . " Business Updates Completed an underwritten public offering of 23,676,471 common shares of the Company for gross proceeds of $ 805 million . Net proceeds from the offering were approximately $ 757.9 million , after deducting underwriting discounts and commissions and other offering expenses payable by the Company . ■ Launched Wired for Worry , a new healthcare provider disease education platform designed to deepen understanding of GAD , reinforce the importance of ongoing assessment , and help healthcare professionals better understand the neurobiological mechanisms that may contribute to the disorder . Program Status and Anticipated Milestones
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Announced positive topline results from Phase 3 Emerge study (MDD) with 149 participants randomized 1:1 to receive DT120 ODT 100 µg or placebo. Key findings included: Met the primary endpoint and all key secondary efficacy endpoints with a high degree of statistical significance. Demonstrated a statistically significant and clinically meaningful placebo-adjusted improvement of 8.1 points in Montgomery-Åsberg Depression Rating Scale (MADRS) total score from baseline at Week 6 (Cohen’s d = 0.83; p<0.0001), the study's primary endpoint. Demonstrated a statistically significant placebo-adjusted improvement of 7.3 points in MADRS total score from baseline at Week 12 (p<0.0001), the study’s key secondary endpoint. DT120 ODT was generally well tolerated, with no serious adverse events and no suicidality signal observed. Completed enrollment of Phase 3 Voyage study (GAD) with 214 participants randomized 1:1 to receive DT120 ODT 100 µg or placebo. Topline data anticipated the week of August 10, 2026. Completed enrollment of Phase 3 Panorama study (GAD) with 245 participants randomized 2:1:2 to receive DT120 ODT 100 µg, DT120 ODT 50 µg control, or placebo. Topline data anticipated in September 2026. Initiated enrollment of Phase 3 Ascend study (MDD). The trial is expected to enroll approximately 165 participants randomized 2:1:2 to receive DT120 ODT 100 µg, DT120 ODT 50 µg control, or placebo. Topline data expected in 2027. Phase 3 Haven study in posttraumatic stress disorder (PTSD) is expected to initiate in 2027 and enroll approximately 200 participants randomized 1:1 to receive DT120 ODT 100 µg or placebo. The primary endpoint in the study is expected to be the Clinician- Administered PTSD Scale for DSM-5 (CAPS-5) at Week 8. Second Quarter 2026 Financial Results Cash, Cash Equivalents and Investments. As of June 30, 2026, Definium Therapeutics had cash, cash equivalents and investments of approximately $1.1 billion compared to $411.6 million as of December 31, 2025. Based on the Company’s current operating plan and anticipated milestones, the Company believes that its cash, cash equivalents and investments as of June 30, 2026 will be sufficient to fund the Company’s operations into 2030. Research and Development (R&D). R&D expenses were $48.7 million for the three months ended June 30, 2026 compared to $29.8 million for the three months ended June 30, 2025, an increase of $18.9 million. The increase was primarily due to an increase of $12.9 million in expenses related to our DT120 program, an increase of $5.7 million in internal personnel costs as a result of increasing research and development capabilities, and an increase of $0.6 million in preclinical and other program expenses, partially offset by a decrease of $0.3 million in DT402 program expenses. General and Administrative (G&A). G&A expenses were $26.4 million for the three months ended June 30, 2026, compared to $11.1 million for the three months ended June 30, 2025, an increase of $15.3 million. The increase was primarily due to an increase of $7.6 million in stock-based compensation expenses, an increase of $2.6 million in corporate and government affairs expenses, an increase of $2.0 million in personnel-related expenses, an increase of $1.8 million in commercial-preparedness related expenses, an increase of $0.6
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million in legal and patent expenses, and an increase of $0.7 million in other miscellaneous administrative expenses. Net loss. Net loss for the three months ended June 30, 2026 was significantly impacted by an $86.2 million non-cash increase in the fair value of warrant liabilities associated with the appreciation in the Company's share price during the period. Net loss for the three months ended June 30, 2026 was $159.0 million, compared to $42.7 million for the three months ended June 30, 2025. Conference Call and Webcast Reminder Definium Therapeutics management will host a webcast at 4:30 p.m. EDT today to provide a corporate update and review the Company’s second quarter 2026 financial results and business highlights. Listeners can register for the webcast via this link. The webcast will be available via the Investor Relations section of the Definium Therapeutics website, ir.definiumtx.com, and archived for at least 30 days after the webcast. Those who plan on participating are advised to join 15 minutes prior to the start time. About DT120 Orally Disintegrating Tablet (ODT) DT120 ODT (lysergide tartrate) is an ergoline derivative belonging to the group of classic serotonergic psychedelics which acts as a partial agonist at serotonin-2A (5-HT2A) receptors. DT120 ODT is Definium’s proprietary and pharmaceutically optimized formulation of LSD. DT120 ODT is an advanced formulation incorporating Catalent’s Zydis® ODT fast- dissolve technology, designed to deliver several unique advantages, including faster absorption and faster onset of transient cognitive, perceptual, and affective changes, improved bioavailability, and lower incidence of gastrointestinal side effects. Definium is developing DT120, the tartrate salt form of lysergide, for generalized anxiety disorder (GAD), major depressive disorder (MDD), posttraumatic stress disorder (PTSD), and is exploring its potential applications in other serious brain health disorders. Definium maintains a strong foundation to protect and extend the long-term value of the DT120 ODT franchise through a multi-layered intellectual property strategy spanning composition, formulation, and methods- of-use patents. About Definium Therapeutics The mission of Definium Therapeutics is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale. Guided by a recognition that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX. For more information, visit www.definiumtx.com and follow Definium Therapeutics on Instagram, LinkedIn and X. Forward-Looking Statements Certain statements in this news release related to the Company constitute "forward-looking information" within the meaning of applicable securities laws and are prospective in nature. Forward-looking information is not based on historical facts, but rather on current expectations and projections about future events and are therefore subject to risks and uncertainties which could cause actual results to differ materially from the future results expressed or implied by the forward-looking statements. These statements generally can be
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identified by the use of forward-looking words such as "will", "may", "should", "could", "intend", "estimate", "plan", "anticipate", "expect", "believe", "potential" or "continue", or the negative thereof or similar variations. Forward-looking information in this news release includes, but is not limited to, statements regarding the Company’s belief in DT120 ODT’s potential to become a best-in-class treatment across multiple psychiatric disorders; the Company’s anticipated topline readout (Part A results) for the Phase 3 Voyage study of DT120 ODT in GAD the week of August 10, 2026; the Company’s anticipated topline readout (Part A results) for the Phase 3 Panorama study for DT120 ODT in GAD in September 2026; the Company’s anticipated topline readout (Part A results) for the Phase 3 Ascend study for DT120 ODT in MDD in 2027; the Company’s expectations regarding enrollment for each of the Haven and Ascend studies; the Company’s expectations to initiate the Haven study in 2027; the Company’s planned trial design for Ascend and Haven; the Company’s beliefs regarding potential benefits of its product candidates; the Company’s expectation that its cash, cash equivalents and investments will fund operations into 2030; and potential additional indications for DT120 ODT. There are numerous risks and uncertainties that could cause actual results and the Company's plans and objectives to differ materially from those expressed in the forward-looking information, including history of negative cash flows; limited operating history; incurrence of future losses; availability of additional capital; compliance with laws and regulations; legislative and regulatory developments, including decisions by the Drug Enforcement Administration and states to reschedule any of our product candidates, if approved, containing Schedule I controlled substances, before they may be legally marketed in the U.S.; difficulty associated with research and development; risks associated with clinical studies or studies; heightened regulatory scrutiny; early stage product development; clinical study risks; regulatory approval processes; novelty of the psychedelic inspired medicines industry; ability to maintain effective patent rights and other intellectual property protection; as well as those risk factors discussed or referred to herein and the risks, uncertainties and other factors described in the Company's Annual Report on Form 10-K for the fiscal year ended December 31, 2025 and its Quarterly Reports on Form 10-Q for the fiscal quarters ended March 31, 2026 and June 30, 2026 under headings such as "Special Note Regarding Forward-Looking Statements," and "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" and other filings and furnishings made or to be made by the Company with the securities regulatory authorities in all provinces and territories of Canada which are available under the Company's profile on SEDAR+ at www.sedarplus.ca and with the U.S. Securities and Exchange Commission on EDGAR at www.sec.gov. Except as required by law, the Company undertakes no duty or obligation to update any forward-looking statements contained in this release as a result of new information, future events, changes in expectations or otherwise.
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Definium Therapeutics, Inc. Consolidated Balance Sheets (in thousands, except share amounts) June 30, 2026 (unaudited) December 31, 2025 Assets Current assets: Cash and cash equivalents $ 655,267 $ 257,837 Short-term investments 428,612 153,756 Prepaid and other current assets 8,222 7,727 Total current assets 1,092,101 419,320 Goodwill 19,918 19,918 Other non-current assets 880 862 Total assets $ 1,112,899 $ 440,100 Liabilities and Shareholders’ Equity Current liabilities: Accounts payable $ 6,965 $ 5,347 Accrued expenses 37,222 20,446 2022 USD Financing Warrants 113,017 40,905 Total current liabilities 157,204 66,698 Credit facility, long-term 36,467 40,579 Other non-current liabilities 549 496 Total liabilities 194,220 107,773 Commitments and contingencies Shareholders' equity: Common shares, no par value, unlimited authorized as of June 30, 2026 and December 31, 2025; 134,365,950 and 98,776,265 issued and outstanding as of June 30, 2026 and December 31, 2025, respectively — — Additional paid-in capital 1,737,018 913,914 Accumulated other comprehensive income 417 1,085 Accumulated deficit (818,756) (582,672) Total shareholders' equity 918,679 332,327 Total liabilities and shareholders' equity $ 1,112,899 $ 440,100
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Definium Therapeutics, Inc. Consolidated Statements of Operations and Comprehensive Loss (unaudited) Three Months Ended June 30,Six Months Ended June 30, (in thousands, except share and per share amounts)2026 2025 2026 2025 Operating expenses: Research and development $ 48,665 $ 29,809 $ 90,149 $ 53,166 General and administrative 26,412 11,094 44,148 19,896 Total operating expenses 75,077 40,903 134,297 73,062 Loss from operations (75,077) (40,903) (134,297) (73,062) Other income/(expense): Interest income 3,587 2,774 7,044 5,207 Interest expense (1,233) (2,338) (2,478) (2,940) Foreign exchange loss, net (32) (49) (76) (68) Change in fair value of 2022 USD Financing Warrants (86,231) (2,228) (106,277) 4,771 Total other income/(expense) (83,909) (1,841) (101,787) 6,970 Net loss (158,986) (42,744) (236,084) (66,092) Other comprehensive loss Unrealized gain/(loss) on investments (406) 36 (668) 46 Loss on foreign currency translation (1) (31) — (58) Comprehensive loss $ (159,393) $ (42,739) $ (236,752) $ (66,104) Net loss per common share, basic $ (1.44) $ (0.50) $ (2.15) $ (0.78) Net loss per common share, diluted $ (1.44) $ (0.50) $ (2.15) $ (0.81) Weighted-average common shares, basic 110,684,720 85,347,677 109,743,062 85,208,539 Weighted-average common shares, diluted 110,684,720 85,347,677 109,743,062 87,099,006 View source version on businesswire.com: https://www.businesswire.com/news/home/20260806201575/en/ For further information, please contact: Investors: Gitanjali Jain VP, Head of Investor Relations ir@definiumtx.com Media: media@definiumtx.com Source: Definium Therapeutics, Inc.