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FLNANasdaq

Filana Therapeutics Inc.

Biopharma developer (SEC filing verified)·Commercial·Austin, TX, United States·CEO: Mr. Richard Jon Barry
OncologyRare DiseaseGene TherapyNeurologyImmunologyCardiovascularInfectious DiseaseMetabolicPainDermatologyHematologyNephrologyMusculoskeletalReproductivePsychiatry

FLNA evidence brief

What we can confirm

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What to watch

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Prepared research question

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

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BioSniper AI · FLNA

Filana Therapeutics Inc. (FLNA) is a clinical-stage biopharmaceutical company focused on developing investigational drug candidates, with a current cash position of $86.6M as of March 31, 2026, and a history of financing operations through public and private stock offerings.

Key risk: No approved products or revenue

7.9/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$44.9M

Cash Runway

29.4 mo

Financial data as of Mar 31, 2026.

Tracking 2 pipeline candidates · 124 clinical trials · 7 catalysts for Filana Therapeutics Inc..

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AI OverviewAI overview is shown in English only.

Filana Therapeutics Inc. (FLNA) is a clinical-stage biopharmaceutical company focused on developing investigational drug candidates, with a current cash position of $86.6M as of March 31, 2026, and a history of financing operations through public and private stock offerings.

  • Cash and equivalents of $86.6M as of March 31, 2026 [sec].
  • Net loss of $10.3M for the quarter ended March 31, 2026 [sec].
  • Shareholders' equity of $74.4M as of March 31, 2026 [sec].
  • Research and development expenses were $4.5M for Q1 2026, down from $13.7M in Q1 2025 [sec_mda · as of 2026-05-07].
  • Company believes current cash will fund operations for at least the next 12 months [sec_mda · as of 2026-05-07].

What works

  • Cash runway of at least 12 months based on current cash and planned spending [sec_mda · as of 2026-05-07].
  • Reduction in R&D expenses from $13.7M to $4.5M year-over-year in Q1 2026 may indicate improved capital efficiency [sec_mda · as of 2026-05-07].
  • Multiple clinical-stage programs with active or completed trials across various indications, including CAR-T and oncology [catalyst].

What to weigh

  • Net loss of $10.3M in Q1 2026 indicates ongoing cash burn [sec].
  • No approved products or revenue streams mentioned in the provided data [sec].
  • Several clinical trials have been terminated, including a Phase 3 Alzheimer's study (NCT05026177) and a simufilam long-term extension study (NCT05575076) [catalyst].
  • Reliance on future financing, with no assurances that additional funding will be available on favorable terms [sec_mda · as of 2026-05-07].

From the filings

Quoted directly from source documents.

  • R&D expenses for Q1 2026

    Research and development expenses were $4.5 million and $13.7 million during the three months ended March 31, 2026 and 2025, respectively.

    SEC MD&A · May 7, 2026

  • Cash runway guidance

    We believe that our current cash and cash equivalents will be sufficient to fund our operations for at least the next 12 months.

    SEC MD&A · May 7, 2026

Catalyst timeline

  • 2026-10-01 · Phase2_StartA multicenter, open-label, randomized controlled clinical study comparing efficacy and safety of an investigational therapy.
  • 2026-10-17 · Phase3_ToplineTopline results for haploidentical allogeneic peripheral blood transplantation trial.
  • 2027-03-01 · Phase3_ToplineTopline results for a randomized double-blind double-dummy trial comparing rituximab versus control.
  • 2032-03-01 · Phase3_ToplineTopline results for TBI-1301 (mipetresgene autoleucel) in NY-ESO-1 positive patients.
Risks & what to watch (4)

Key risks

  • No approved products or revenueCompany has no marketed products or reported revenue, relying solely on financing and collaborations [sec].
  • Clinical trial terminationsSeveral Phase 3 trials, including Alzheimer's and simufilam studies, have been terminated [catalyst].
  • Future financing uncertaintyNo assurance that additional funding will be available on favorable terms [sec_mda · as of 2026-05-07].
  • Dependence on investigational candidatesAll assets are investigational and subject to regulatory approval risks [sec · filed 2025-08-04].

What to watch

  • Upcoming Phase 2 start on 2026-10-01 for a multicenter randomized controlled study [catalyst].
  • Phase 3 topline results for haploidentical transplantation on 2026-10-17 [catalyst].
  • Phase 3 topline for rituximab combination on 2027-03-01 [catalyst].
  • Phase 3 topline for TBI-1301 (mipetresgene autoleucel) on 2032-03-01 [catalyst].

Sources: Catalysts · SEC filings · SEC MD&A · Generated August 28, 2026 · How we verify sources →

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Evidence & data

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

Cash Runway8.2

29.4 months

Financial Health8.2

D/E 0.59

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth4.6

2 candidates

Catalyst Momentum10.0

7 upcoming, next in ~32d

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

100

Total value held

$26.2M

Showing top 10 of 100 institutional holders of Filana Therapeutics Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 12, 2026
% of float
14.6%
Days to cover
19.0
Shares short
6,925,885
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 →

FLNA short interest

Governance

Frequently asked questions

What is the AI investment thesis for Filana Therapeutics Inc.?

Filana Therapeutics Inc. (FLNA) is a clinical-stage biopharmaceutical company focused on developing investigational drug candidates, with a current cash position of $86.6M as of March 31, 2026, and a history of financing operations through public and private stock offerings.

What is Filana Therapeutics Inc.'s lead drug candidate?

Filana Therapeutics Inc.'s most advanced tracked candidate is simufilam (Phase 3) for Alzheimer Disease; Alzheimer's Disease; Absorption.

What is Filana Therapeutics Inc.'s next catalyst?

Filana Therapeutics Inc.'s next tracked catalyst is a Phase2_Start event — "Phase 2 Start: A Multicenter, Open-label, Randomized Controlled Clinical Study Comparing the Efficacy and Safety of" — expected October 1, 2026.

Who is the CEO of Filana Therapeutics Inc.?

Mr. Richard Jon Barry is the chief executive officer of Filana Therapeutics Inc. (FLNA).

Where is Filana Therapeutics Inc. headquartered?

Filana Therapeutics Inc. (FLNA) is headquartered in Austin, TX, 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.