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NERVNasdaq

Minerva Neurosciences, Inc.

Pharmaceutical preparations·Phase 3·Burlington, MA, United States·CEO: Dr. Remy Luthringer Ph.D.
NeurologyImmunology

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BioSniper AI · NERV

Minerva Neurosciences, Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for central nervous system (CNS) diseases, with its lead candidate roluperidone in Phase 3 trials for negative symptoms in schizophrenia.

Key risk: Clinical trial failure risk

4.1/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$231.1M

Cash Runway

16.7 mo

Lead Asset

roluperidone (Phase 3)

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 3 clinical trials · 1 catalyst for Minerva Neurosciences, Inc..

AI OverviewAI overview is shown in English only.

Minerva Neurosciences, Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for central nervous system (CNS) diseases, with its lead candidate roluperidone in Phase 3 trials for negative symptoms in schizophrenia.

  • Lead candidate roluperidone is in a Phase 3 trial for negative symptoms in schizophrenia [sec · filed 2026-05-27].
  • As of June 30, 2026, cash & equivalents were $24.8M, with net income of $17.5M and shareholders' equity of -$32.1M [sec].
  • Accumulated deficit was approximately $796.7 million as of June 30, 2026 [sec_mda · as of 2026-08-07].
  • No products approved for commercial sale and no revenue from product sales to date [sec_mda · as of 2026-08-07].
  • Management believes existing cash will fund operations for at least 12 months from the date of the June 30, 2026 financial statements [sec_mda · as of 2026-08-07].

What works

  • Roluperidone is in a Phase 3 trial targeting negative symptoms in schizophrenia, a high unmet medical need [sec · filed 2026-05-27].
  • Cash position of $24.8M as of June 30, 2026, provides near-term operational runway [sec].
  • Net income of $17.5M in the latest reported period may indicate improved financial management or one-time gains [sec].

What to weigh

  • Accumulated deficit of $796.7M as of June 30, 2026, reflects a long history of losses [sec_mda · as of 2026-08-07].
  • No approved products or product revenue, and the company may never achieve profitability [sec_mda · as of 2026-08-07].
  • Shareholders' equity is negative (-$32.1M as of June 30, 2026), indicating a weak balance sheet [sec].
  • The company will require additional capital to finance operations, which may not be available on acceptable terms [sec_mda · as of 2025-05-13].

From the filings

Quoted directly from source documents.

  • Roluperidone is in Phase 3 for negative symptoms in schizophrenia.

    for the treatment of negative symptoms in schizophrenia.

    SEC filings · May 27, 2026

  • Accumulated deficit as of June 30, 2026.

    had an accumulated deficit of approximately $796.7 million.

    SEC MD&A · August 7, 2026

  • No product revenue to date.

    We have no products approved for commercial sale and have not generated any revenue from product sales to date

    SEC MD&A · August 7, 2026

  • Cash runway of at least 12 months from June 30, 2026.

    we believe will be sufficient to meet our operating commitments for the next 12 months from the date our interim condensed financial statements are issued.

    SEC MD&A · August 7, 2026

Catalyst timeline

  • 2028-12-01 · Phase3_ToplineTopline results from a 12-week, randomized, double-blind, placebo-controlled monotherapy study of roluperidone for negative symptoms in schizophrenia.
Risks & what to watch (4)

Key risks

  • Clinical trial failure riskPhase 3 trial of roluperidone may fail to meet endpoints, delaying or ending development [sec · filed 2026-05-27].
  • Need for additional financingCompany will require additional capital; may not be available on acceptable terms [sec_mda · as of 2025-05-13].
  • No approved products or revenueNo products approved for commercial sale and no product revenue to date [sec_mda · as of 2026-08-07].
  • Regulatory and FDA feedback risksInteractions with FDA may affect trial design, timeline, or approval [sec · filed 2026-05-27].

What to watch

  • Phase 3 topline data for roluperidone expected December 1, 2028 [catalyst].
  • Cash runway and any additional financing activities [sec_mda · as of 2026-08-07].
  • FDA feedback on the confirmatory trial design for roluperidone [sec · filed 2026-05-27].
  • Progress toward potential commercialization and revenue generation [sec_mda · as of 2026-08-07].

Sources: SEC filings · SEC MD&A · Generated August 24, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway4.6

16.7 months

Financial Health2.0

OCF -$13M · Net income $17M

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth3.3

1 candidate

Catalyst Momentum2.0

1 upcoming, next in ~824d

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

39

Total value held

$190.4M

Showing top 10 of 39 institutional holders of Minerva Neurosciences, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 30, 2026
% of float
2.8%
Days to cover
2.9
Shares short
1,156,257
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

NERV short interest

Governance

Frequently asked questions

What is the AI investment thesis for Minerva Neurosciences, Inc.?

Minerva Neurosciences, Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for central nervous system (CNS) diseases, with its lead candidate roluperidone in Phase 3 trials for negative symptoms in schizophrenia.

What is Minerva Neurosciences, Inc.'s lead drug candidate?

Minerva Neurosciences, Inc.'s most advanced tracked candidate is roluperidone (Phase 3) for Negative Symptoms of Schizophrenia.

What is Minerva Neurosciences, Inc.'s next catalyst?

Minerva Neurosciences, Inc.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A 12-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Monotherapy Study to Evaluate " — expected December 1, 2028.

Who is the CEO of Minerva Neurosciences, Inc.?

Dr. Remy Luthringer Ph.D. is the chief executive officer of Minerva Neurosciences, Inc. (NERV).

Where is Minerva Neurosciences, Inc. headquartered?

Minerva Neurosciences, Inc. (NERV) is headquartered in Burlington, MA, United States.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.