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Minerva appoints Anthony Aliquo as Chief Accounting Officer; CFO Fred Ahlholm remains
Anthony Aliquo appointed CAO and principal accounting officer effective Aug 10, 2026.
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Minerva Q2 GAAP net income $17.5M on $27.6M non-cash warrant gain; adjusted loss $7.8M
Q2 2026 GAAP net income of $17.5M ($0.36 basic, $(0.14) diluted) vs net loss of $3.3M year-ago; driven by $27.6M non-cash warrant gain.
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Shareholders approve officer exculpation charter amendment; board adopts updated bylaws at annual meeting
Shareholders approved exculpation amendment to limit officer liability for monetary damages to full extent under Delaware law.
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Minerva enters $75M ATM offering; Phase 3 roluperidone relapse phase extended to 52 weeks
Up to $75M in common stock may be sold at-the-market through Leerink Partners; 3% commission.
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Minerva Q1 GAAP net loss $125.4M on warrant revaluation; Phase 3 roluperidone trial advances
Confirmatory Phase 3 trial of roluperidone for negative symptoms of schizophrenia initiated; first patient screened March 2026; topline data expected 2H 2027.
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Minerva Neurosciences sets 2026 annual meeting for June 3; proposal deadlines announced
Annual meeting of stockholders scheduled for June 3, 2026.
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Minerva Neurosciences President resigns; James O'Connor named Chief Business Officer and General Counsel
Geoffrey Race resigned as President effective March 31, 2026 after 16 years with the company.
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Minerva (NERV) Q4 non-GAAP adj loss $7.1M; cash $82.4M; Phase 3 roluperidone on track for Q2 2026
Non-GAAP adjusted net loss for Q4 2025 was $7.1M ($0.64/sh) vs $4.0M ($0.53/sh) in Q4 2024.
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Minerva unveils Phase 3 trial design for roluperidone; planned start Q2 2026
Phase 3 trial to enroll 380 patients with negative symptoms of schizophrenia; 1:1 randomization to placebo or 64 mg roluperidone.
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Minerva Neurosciences stockholders approve increase in authorized common shares to 250M and 12.5M new equity plan shares
Stockholders approved increasing authorized common shares from 125M to 250M. Votes: 4,917,181 for, 314,773 against.
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Minerva Neurosciences appoints Dr. Inderjit Kaul to board; Kaul led Cobenfy schizophrenia program at BMS
Dr. Kaul appointed to Minerva's board (Class II) effective Nov 14, 2025; board size increased to 6.
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Minerva Neurosciences raises up to $200M to fund Phase 3 trial of roluperidone
Private placement: $80M upfront Series A preferred; Tranche A warrants for another $80M (cash exercise), Tranche B warrants for $40M contingent on milestone event.
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Minerva Neurosciences regains Nasdaq compliance with net income rule
Nasdaq Panel confirmed compliance with Listing Rule 5550(b)(3) (minimum $500K net income from continuing operations).
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Nasdaq Panel grants Minerva continued listing subject to equity compliance by March 31, 2025
Company must file disclosure on transactions to meet $2.5M minimum stockholders' equity by 3/31/25.
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Minerva Neurosciences annual meeting vote results: directors elected, say-on-pay approved, auditor ratified
Hans Peter Hasler elected with 3,384,409 For, 353,053 Withheld; Dr. Remy Luthringer elected with 3,705,617 For, 31,845 Withheld (1,624,748 broker non-votes each).
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Minerva Neurosciences receives Nasdaq delisting notice for MVLS non-compliance; to request hearing
Second Nasdaq notice for continued non-compliance with $35M minimum Market Value of Listed Securities; delisting determination unless hearing requested.
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Minerva Neurosciences sets 2024 annual meeting for Dec 5, stockholder deadline Oct 1
Annual meeting scheduled for December 5, 2024, more than 30 days from 2023 meeting anniversary.
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Director Jeryl Hilleman resigns from Minerva Neurosciences Board; Audit Committee roles reassigned
Jeryl Hilleman resigns from Board and Audit Committee Chair, effective August 6, 2024.
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Minerva Neurosciences receives Nasdaq delisting notice for low market value
MVLS below $35M minimum for 31 consecutive business days as of April 10, 2024.
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FDA issues Complete Response Letter for roluperidone; NDA not approved
FDA cited single positive study insufficient; requires at least one additional positive well-controlled trial.
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Minerva Neurosciences stockholders approve all proposals at 2023 annual meeting
Directors David Kupfer and Jan van Heek elected with ~3.25M and ~3.37M votes, respectively.
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Minerva Neurosciences raises $20M in PIPE at $10/share for roluperidone launch
Gross proceeds ~$20M from 1,425,000 shares at $10/share and 575,575 pre-funded warrants at $9.99.
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Minerva Neurosciences regains Nasdaq compliance on minimum market value requirement
Received Nasdaq Compliance Notice on June 16, 2023, after MVLS exceeded $35M for 10 consecutive business days.
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Minerva Neurosciences receives Nasdaq delisting determination; intends to request hearing
Received second Nasdaq notice on May 31 for continued non-compliance with minimum Market Value of Listed Securities ($35M).
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Minerva Neurosciences director William Doyle resigns; board appoints replacements
William Doyle resigned from the Board effective May 3, 2023, including as Chair of Compensation Committee.
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Minerva Neurosciences announces FDA files NDA for roluperidone after appeal of refuse-to-file
FDA filed Minerva's NDA for roluperidone on April 27, 2023, to treat negative symptoms in schizophrenia.
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FDA upholds refusal to file Minerva's NDA for roluperidone for schizophrenia negative symptoms
FDA confirmed refusal-to-file letter dated Oct 14, 2022 remains in effect after Type A meeting on Nov 30, 2022.
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Minerva Neurosciences amends CEO Luthringer's employment agreement with enhanced severance terms
CEO Remy Luthringer to receive 12 months base salary continuation upon termination without cause.
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Minerva Neurosciences receives Nasdaq notice for MVLS non-compliance; has until May 30, 2023
Nasdaq notified Minerva on Dec 1, 2022 that MVLS fell below $35M for 30 consecutive business days.
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Minerva Neurosciences receives FDA refusal to file for roluperidone NDA in schizophrenia negative symptoms
FDA issued Refusal to File letter for NDA of roluperidone for negative symptoms of schizophrenia.
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Minerva Neurosciences transfers stock listing to Nasdaq Capital Market to avoid delisting
Transfer from Nasdaq Global Market to Nasdaq Capital Market effective Sept 12, 2022; ticker NERV unchanged.
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Minerva submits NDA to FDA for roluperidone (64 mg) to treat negative symptoms of schizophrenia
NDA supported by two late-stage studies (MIN-101C03 and MIN-101C07) in patients with moderate to severe negative symptoms.
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Minerva Neurosciences files for 1-for-8 reverse stock split effective June 17, 2022
Stockholders approved reverse split at June 10, 2022 annual meeting; board set ratio at 1-for-8.
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Minerva Neurosciences shareholders approve reverse stock split ratio of 1:4 to 1:10
Reverse stock split authorized by 93.5% of votes cast (25.9M for, 1.7M against).
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Minerva Neurosciences hosts roluperidone update webcast; no specific details in 8-K
Company held an investor webcast on April 13, 2022, to discuss updates on roluperidone.
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FDA says Phase 3 study for roluperidone remains negative; additional data needed
FDA stated the Phase 3 study is negative under the Hochberg procedure; both 32 mg and 64 mg doses must be significant.
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Minerva Neurosciences receives Nasdaq delisting notice for equity shortfall
Notice received March 8, 2022: stockholders' equity in 2021 10-K fails Nasdaq Rule 5450(b)(1).
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Phase 3 roluperidone results published; primary endpoint missed significance in ITT
Trial published in Schizophrenia Bulletin for roluperidone to treat negative symptoms in schizophrenia.
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Minerva Neurosciences receives Nasdaq deficiency notice for bid price below $1.00
Nasdaq letter dated Jan 12, 2022, for closing bid price below $1.00 for 30 consecutive business days.
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Minerva Neurosciences presents corporate update at LifeSci Partners event on Jan 5, 2022
Corporate presentation furnished as Exhibit 99.1 to Form 8-K.
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Roluperidone phase 3 trial: primary endpoint missed in ITT (p=0.064) but significant in mITT; PSP improved
NSFS (primary) for roluperidone 64mg vs placebo: p≤0.064 (ITT), p≤0.044 (mITT).
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FDA denies Minerva's pre-NDA meeting request for roluperidone, recommends Type C meeting
FDA denied pre-NDA meeting for roluperidone (negative symptoms of schizophrenia); recommends Type C guidance meeting instead.
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Minerva Neurosciences promotes Geoff Race to President, Frederick Ahlholm to CFO; pre-NDA meeting planned
Geoff Race promoted to President effective Oct 11, 2021; he was EVP, CFO, and CBO.
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Minerva's roluperidone bioequivalence study meets all PK objectives; pre-NDA meeting planned
Study showed bioequivalence in AUC_inf between Phase 2b, Phase 3, and planned commercial formulations.
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Minerva Neurosciences appoints Dr. Kuchibhatla as SVP Head of R&D; Dr. Saoud to advisory role
Dr. Jay Saoud resigns as SVP Head of R&D effective Sept 15, 2021; transitions to consultant through June 2022.