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MNOVNasdaq

MEDICINOVA INC

Biopharma developer (SEC filing verified)·Phase 2·La Jolla, CA, United States·CEO: Dr. Yuichi Iwaki M.D., Ph.D.
OncologyNeurologyMetabolicRespiratoryGastroenterology

MNOV evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

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BioSniper AIPage evidence connected

Prepared research question

What matters most for MNOV—catalysts, financial risk and supporting evidence?

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BioSniper AI · MNOV

Medicinova Inc is a biopharmaceutical company focused on developing novel therapeutics for serious diseases with unmet medical needs, with a commercial focus on the U.S. market and a key upcoming Phase 3 topline readout in 2028.

Key risk: Capital dependency

7.0/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$70.6M

Cash Runway

39.9 mo

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 4 clinical trials · 1 catalyst for MEDICINOVA INC.

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AI OverviewAI overview is shown in English only.

Medicinova Inc is a biopharmaceutical company focused on developing novel therapeutics for serious diseases with unmet medical needs, with a commercial focus on the U.S. market and a key upcoming Phase 3 topline readout in 2028.

  • Medicinova is a biopharmaceutical company focused on developing novel therapeutics for serious diseases with unmet medical needs, with a commercial focus on the U.S. market [sec_mda · as of 2026-03-10].
  • As of 2026-06-30, the company reported cash & equivalents of $25.4M, total revenue of $0.5M, net income of -$2.3M, and shareholders' equity of $41.6M [sec].
  • The company faces risks including inability to raise additional capital, generate product revenues, or complete clinical trials and obtain regulatory approval [sec_mda · as of 2026-08-13].
  • A Phase 3 topline readout is scheduled for 2028-04-01, from a randomized, double-blind, placebo-controlled 12-month clinical trial [upcoming catalysts].

What works

  • The company has a focused strategy on novel therapeutics for serious diseases with unmet medical needs, targeting a clear market opportunity [sec_mda · as of 2026-03-10].
  • Shareholders' equity of $41.6M as of 2026-06-30 provides a capital base to support ongoing operations and clinical development [sec].

What to weigh

  • The company has minimal revenue ($0.5M as of 2026-06-30) and is not yet generating product sales, relying on external capital to fund operations [sec].
  • The company faces significant risks including inability to raise additional capital, complete clinical trials, or obtain FDA approval, which could materially affect future results [sec_mda · as of 2026-08-13].
  • Net loss of $2.3M as of 2026-06-30 indicates ongoing cash burn without a clear path to profitability [sec].

From the filings

Quoted directly from source documents.

  • Company focus on novel therapeutics for serious diseases with unmet medical needs

    We are a biopharmaceutical company focused on developing novel therapeutics for the treatment of serious diseases with unmet medical needs and a commercial focus on the United States market.

    SEC MD&A · March 10, 2026

  • Risks include inability to raise capital, generate revenues, and complete clinical trials

    Inability to raise additional capital if needed; • Inability to generate revenues from product sales to continue business operations; • Inability to develop and commercialize our product candidates; • Failure or delay in completing clinical trials or obtaining Food and Drug Administration or foreign regulatory approval for our product candidates in a timely manner

    SEC MD&A · August 13, 2026

Catalyst timeline

  • 2028-04-01 · Phase3_ToplineTopline results from a Phase 2b/3 randomized, double-blind, placebo-controlled 12-month clinical trial will be reported, providing key efficacy and safety data.
Risks & what to watch (3)

Key risks

  • Capital dependencyInability to raise additional capital if needed, as the company has minimal revenue and ongoing net losses [sec_mda · as of 2026-08-13].
  • Clinical and regulatory failureFailure or delay in completing clinical trials or obtaining FDA approval for product candidates [sec_mda · as of 2026-08-13].
  • Revenue generation riskInability to generate revenues from product sales to continue business operations [sec_mda · as of 2026-08-13].

What to watch

  • Phase 3 topline readout expected on 2028-04-01, which will be a key determinant of the company's clinical and regulatory trajectory [upcoming catalysts].
  • Cash runway and ability to raise additional capital, given the company's net loss and limited revenue [sec].
  • Any updates on FDA interactions or regulatory milestones for the lead candidate [sec_mda · as of 2026-08-13].

Sources: SEC MD&A · Generated August 29, 2026 · How we verify sources →

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Evidence & data

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

Cash Runway10.0

39.9 months

Financial Health9.9

D/E 0.08 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 1/Phase 2

Pipeline Breadth7.2

4 candidates

Catalyst Momentum2.0

1 upcoming, next in ~580d

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

29

Total value held

$7.9M

Showing top 10 of 29 institutional holders of MEDICINOVA INC. Open the full 13F history after sign-in.

Short Interest

as of May 21, 2026
% of float
0.4%
Days to cover
6.3
Shares short
172,326
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 →

MNOV short interest

Governance

Frequently asked questions

What is the AI investment thesis for MEDICINOVA INC?

Medicinova Inc is a biopharmaceutical company focused on developing novel therapeutics for serious diseases with unmet medical needs, with a commercial focus on the U.S. market and a key upcoming Phase 3 topline readout in 2028.

What is MEDICINOVA INC's lead drug candidate?

MEDICINOVA INC's most advanced tracked candidate is mn-001 (Phase 2) for Diabetes Mellitus, Type 2; Idiopathic Pulmonary Fibrosis.

What is MEDICINOVA INC's next catalyst?

MEDICINOVA INC's next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A Phase 2b/3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, 12 Month Clinical Trial to" — expected April 1, 2028.

Who is the CEO of MEDICINOVA INC?

Dr. Yuichi Iwaki M.D., Ph.D. is the chief executive officer of MEDICINOVA INC (MNOV).

Where is MEDICINOVA INC headquartered?

MEDICINOVA INC (MNOV) is headquartered in La Jolla, CA, United States.

925 companies232,681 SEC filings21,419 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.