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TYRANasdaq

Tyra Biosciences, Inc.

Pharmaceutical preparations·Phase 2·Carlsbad, CA, United States·CEO: Dr. Todd Harris Ph.D.
OncologyRare Disease

TYRA evidence brief

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What it means

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

What to watch

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Prepared research question

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

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BioSniper AI · TYRA

Tyra Biosciences, Inc. (TYRA) is a clinical-stage biopharmaceutical company focused on developing precision therapies for genetically defined cancers, with three product candidates in clinical development and no approved products.

Key risk: No approved products or revenue

5.8/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$1.48B

Cash Runway

15.7 mo

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 8 clinical trials · 1 catalyst for Tyra Biosciences, Inc..

AI OverviewAI overview is shown in English only.

Tyra Biosciences, Inc. (TYRA) is a clinical-stage biopharmaceutical company focused on developing precision therapies for genetically defined cancers, with three product candidates in clinical development and no approved products.

  • Tyra Biosciences has three product candidates in clinical development, with other programs in preclinical or discovery stages [sec_mda · as of 2026-03-02].
  • As of June 30, 2026, the company had cash, cash equivalents and marketable securities of $353.9 million and an accumulated deficit of $456.1 million [sec_mda · as of 2026-08-04].
  • The company has not generated any revenue to date and has funded operations primarily through its initial public offering and private placements [sec_mda · as of 2025-08-14].
  • Tyra has never completed any clinical trials or submitted an application for marketing approval for any product candidate [sec_mda · as of 2026-03-02].

What works

  • Cash, cash equivalents and marketable securities of $353.9 million as of June 30, 2026, provides a substantial runway to advance clinical programs [sec_mda · as of 2026-08-04].
  • The company is advancing three product candidates in clinical development, including dabogratinib, which is being evaluated in a Phase 2 trial for FGFR2-driven intrahepatic cholangiocarcinoma [sec_mda · as of 2025-08-14].
  • Tyra's proprietary SNÅP platform supports ongoing research and development activities for future product candidates [sec_mda · as of 2025-08-14].

What to weigh

  • Tyra has an accumulated deficit of $456.1 million as of June 30, 2026, and expects to continue incurring significant operating losses for the foreseeable future [sec_mda · as of 2026-08-04].
  • The company has no products approved for commercial sale and has never completed a clinical trial or submitted a marketing application, making its business highly speculative [sec_mda · as of 2026-03-02].
  • Future capital requirements are uncertain and depend on many factors, including the timing and costs of clinical trials, which could deplete resources sooner than expected [sec_mda · as of 2026-05-13].

From the filings

Quoted directly from source documents.

  • Tyra has three product candidates in clinical development and other programs in preclinical or discovery stages.

    We have three product candidates in clinical development. Our other development programs are either in preclinical development or in the drug discovery stage.

    SEC MD&A · March 2, 2026

  • As of June 30, 2026, Tyra had $353.9 million in cash, cash equivalents and marketable securities.

    As of June 30, 2026, we had cash, cash equivalents and marketable securities of $353.9 million.

    SEC MD&A · August 4, 2026

  • Tyra has an accumulated deficit of $456.1 million as of June 30, 2026.

    had an accumulated deficit of $456.1 million.

    SEC MD&A · August 4, 2026

  • Tyra has never completed any clinical trials or submitted a marketing application.

    As an organization, we have never completed any clinical trials or submitted an application for marketing approval and may be unable to do so for any of our product candidates.

    SEC MD&A · March 2, 2026

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · dabogratinib — Phase 2 Readout: dabogratinibTop-line results from the Phase 2 trial of dabogratinib in FGFR2-driven intrahepatic cholangiocarcinoma are expected, which will provide initial efficacy and safety data.
Risks & what to watch (4)

Key risks

  • No approved products or revenueTyra has no products approved for commercial sale and has not generated any revenue to date [sec_mda · as of 2025-08-14].
  • Significant accumulated deficitAccumulated deficit of $456.1 million as of June 30, 2026, with expected continued losses [sec_mda · as of 2026-08-04].
  • Clinical development uncertaintyThe company has never completed a clinical trial, and results may not support regulatory approval [sec_mda · as of 2026-03-02].
  • Capital depletion riskFuture capital requirements are uncertain and could deplete resources sooner than expected [sec_mda · as of 2026-05-13].

What to watch

  • Phase 2 top-line data for dabogratinib in FGFR2-driven intrahepatic cholangiocarcinoma, expected by the end of 2026 [catalyst_timeline].
  • Progress of the other two clinical-stage product candidates and any updates on preclinical programs [sec_mda · as of 2026-03-02].
  • Changes in cash runway and operating expenses as clinical activities expand [sec_mda · as of 2026-08-04].

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

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Evidence & data

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

Cash Runway4.4

15.7 months

Financial Health9.9

D/E 0.08 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth7.2

4 candidates

Catalyst Momentum3.0

1 upcoming, next in ~123d

Insider Signal4.3

0 buys · 1 sell (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

160

Total value held

$2.20B

HolderSharesValue
ra capital management, l.p.12,198,625$467.2M
janus henderson group plc7,781,178$297.7M
fmr llc7,747,648$296.7M
farallon capital management llc3,580,818$137.1M
commodore capital lp2,475,000$94.8M
vanguard capital management llc2,251,940$86.2M
blackrock, inc.2,217,929$84.9M
bvf inc/il1,976,196$75.7M
caligan partners lp1,276,968$48.9M
state street corp1,216,078$46.6M

Showing top 10 of 160 institutional holders of Tyra Biosciences, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 19, 2026
% of float
22.4%
Days to cover
6.2
Shares short
8,264,887
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 →

TYRA short interest

Governance

Frequently asked questions

What is the AI investment thesis for Tyra Biosciences, Inc.?

Tyra Biosciences, Inc. (TYRA) is a clinical-stage biopharmaceutical company focused on developing precision therapies for genetically defined cancers, with three product candidates in clinical development and no approved products.

What is Tyra Biosciences, Inc.'s lead drug candidate?

Tyra Biosciences, Inc.'s most advanced tracked candidate is dabogratinib (Phase 2) for Low Grade Upper Tract Urothelial Carcinoma.

What is Tyra Biosciences, Inc.'s next catalyst?

Tyra Biosciences, Inc.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: dabogratinib" — expected December 31, 2026.

Who is the CEO of Tyra Biosciences, Inc.?

Dr. Todd Harris Ph.D. is the chief executive officer of Tyra Biosciences, Inc. (TYRA).

Where is Tyra Biosciences, Inc. headquartered?

Tyra Biosciences, Inc. (TYRA) is headquartered in Carlsbad, 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.