Tyra Biosciences
Tyra Biosciences is a clinical-stage biotech developing oral FGFR-selective precision medicines, led by dabogratinib (FGFR3) for bladder cancer, upper tract urothelial carcinoma, and pediatric achondroplasia, using its proprietary SNÅP structure-based drug design platform.
- Company typePublic
- Founded2018
- HeadquartersCarlsbad, United States
- Headcount101–250
- GTM typeB2B
- OfferingHardware or Manufacturing
What Tyra Biosciences does
Tyra Biosciences is a clinical-stage biotechnology company developing next-generation precision medicines targeting FGFR biology in oncology and genetically defined conditions. The company was founded in 2018 and is headquartered in Carlsbad, California, listed on Nasdaq under the ticker TYRA since its 2021 IPO. Its core technology is the proprietary SNÅP Discovery Engine, an in-house structure-based drug design platform that produces full co-crystal structural "SNÅPshots" of drug-target interactions in as little as seven days, enabling angstrom-level medicinal chemistry iteration against a backdrop of hundreds of internally solved FGFR crystal structures.
The pipeline centers on three investigational oral FGFR inhibitors. The lead asset, dabogratinib (formerly TYRA-300), is a selective FGFR3 inhibitor designed to retain activity against the V555 gatekeeper resistance mutation and to avoid FGFR1-mediated off-target toxicity; it is being advanced concurrently in three Phase 2 studies under a "3x3" strategy: SURF302 in FGFR3-altered intermediate-risk non-muscle invasive bladder cancer (IR NMIBC), SURF303 in low-grade upper tract urothelial carcinoma (LG-UTUC), and BEACH301 in pediatric achondroplasia. Two additional candidates — TYRA-430, an FGFR4/3-biased inhibitor in the Phase 1 SURF431 study for FGF19+/FGFR4-driven hepatocellular carcinoma, and TYRA-200, an FGFR1/2/3 inhibitor in the Phase 1 SURF201 study for FGFR2-altered cholangiocarcinoma — extend the platform.
The business is pre-revenue, funded entirely through capital markets, with no commercial product. As of Q1 2026, Tyra held $383.5M in cash and securities providing runway into the second half of 2028; R&D spend in Q1 2026 was $33.5M (up from $25.0M a year earlier) and full-year 2025 net loss was $119.9M. Commercial launch is anticipated post-approval, supported by a leadership team specifically built for rare-oncology and rare-disease commercialization.
Tyra Biosciences firmographics
Firmographics- Name
- Tyra Biosciences
- Legal name
- Tyra Biosciences, Inc.
- Website
- https://tyra.bio/
- Company type
- Public
- Founded year
- 2018
- Operating status
- Operating
- Headcount range
- 101–250 employees
- Short description
- Tyra Biosciences is a clinical-stage biotech developing oral FGFR-selective precision medicines, led by dabogratinib (FGFR3) for bladder cancer, upper tract urothelial carcinoma, and pediatric achondroplasia, using its proprietary SNÅP structure-based drug design platform.
- Ownership category
- akta.pro rank
Tyra Biosciences industry classification
Industry- Product category
- Precision Oncology Pharmaceuticals
- NAICS
- Research and Development in Biotechnology (except Nanobiotechnology) (541714), Pharmaceutical and Medicine Manufacturing (3254)
- SIC
- Pharmaceutical Preparations (2834), Medicinal Chemicals & Botanical Products (2833)
- akta.pro primary industry
- Drug Discovery (Target ID/Validation & Hit Discovery) (HLAIALAA)
- akta.pro secondary industry
- Translational Medicine & Biomarkers (HLAIALAF)
Keywords
Where Tyra Biosciences is headquartered
LocationHeadquarters
- HQ city
- Carlsbad
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Tyra Biosciences business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales
Revenue model
- Pre-revenue clinical-stage pipeline: Tyra Biosciences is a clinical-stage biotechnology company with no commercial product revenue. Net loss was $119.9 million for full-year 2025 and $39.3 million for Q1 2026, with R&D expenses increasing to $33.5 million from $25.0 million year-over-year. The company is funded by capital markets and expects no product revenue until regulatory approval and commercialization of dabogratinib, TYRA-200, or TYRA-430.
- Capital markets financing (future R&D monetization): Pre-revenue biotech funded through equity financings including a $200 million private placement (Feb 2024), a $126 million at-the-market offering (March 2026), and prior IPO proceeds. These proceeds fund clinical development that will eventually translate to pharmaceutical product sales (likely one-time license / direct sales once approved).
Go-to-market motion1 record
Distribution channels1 record
Marketing channels7 records
Tyra Biosciences product offering
Product offeringCore offering
Tyra Biosciences is a clinical-stage biotechnology company that develops investigational, oral small-molecule precision medicines targeting fibroblast growth factor receptor (FGFR) biology for oncology and genetically defined conditions. The company is advancing three drug candidates — dabogratinib (FGFR3-selective), TYRA-430 (FGFR4/3-biased), and TYRA-200 (FGFR1/2/3) — designed using its proprietary SNAP Discovery Engine to overcome acquired resistance and improve isoform selectivity relative to first-generation FGFR inhibitors.
Product overview
Tyra Biosciences is a clinical-stage biotechnology company that develops next-generation precision medicines using its proprietary SNAP Discovery Engine, a structure-based drug design platform built around hundreds of internally solved FGFR co-crystal structures. The company offers a focused portfolio of three investigational small-molecule precision oncology and skeletal-dysplasia drug candidates — the lead asset dabogratinib (formerly TYRA-300), a selective FGFR3 inhibitor being advanced in three Phase 2 studies (BEACH301 for achondroplasia, SURF302 for IR NMIBC, and SURF303 for LG-UTUC); TYRA-430, an FGFR4/3-biased inhibitor in the Phase 1 SURF431 study for FGF19+/FGFR4-driven hepatocellular carcinoma and other solid tumors; and TYRA-200, an FGFR1/2/3 inhibitor in the Phase 1 SURF201 study for FGFR2-altered cholangiocarcinoma and other solid tumors. Together, the SNAP engine and the three FGFR-targeted product candidates form an integrated precision-medicine platform targeting FGFR biology across oncology and genetically defined conditions.
Differentiator
Problem solved
Functional benefit
Brands
- dabogratinib: Lead product candidate, an investigational selective FGFR3 inhibitor formerly known as TYRA-300; being developed across skeletal dysplasia (achondroplasia), bladder cancer (NMIBC), and LG-UTUC indications.
- TYRA-430
- TYRA-200
- SNAP (SNÅP) Discovery Engine
Products and services
- Dabogratinib (formerly TYRA-300) Investigational oral, selective inhibitor of FGFR3 designed to maintain potency in the presence of treatment-emergent resistance mutations such as the V555 gatekeeper mutation and to be selective for FGFR3 over FGFR1/2 to limit off-target toxicity. Being developed for achondroplasia (BEACH301), intermediate-risk non-muscle invasive bladder cancer (SURF302), and low-grade upper tract urothelial carcinoma (SURF303).
- TYRA-430 Investigational oral FGFR4/3-biased inhibitor designed for FGF19+/FGFR4-driven cancers including advanced hepatocellular carcinoma (HCC), providing isoform-selective targeting. Currently in the SURF431 Phase 1 multicenter, open-label, first-in-human study.
- TYRA-200 Investigational oral FGFR1/2/3 inhibitor that has demonstrated in vitro potency against activating FGFR2 gene alterations and resistance mutations. Being evaluated in the SURF201 Phase 1 study for adults with unresectable locally advanced/metastatic intrahepatic cholangiocarcinoma and other advanced solid tumors with activating FGFR2 alterations.
Quantifiable outcome
- Q1 2026 R&D expenses grew to $33.5 million from $25.0 million in Q1 2025, supporting advancement of three Phase 2 programs concurrently.
- +4 more outcomes
Companies that use Tyra Biosciences
Customer profileSegments6 records
Ideal customer profiles2 records
Tyra Biosciences technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature6 records
Tyra Biosciences partnerships and signals
Strategic signalPartnerships
Two partnerships are on record, tiered minor and core.
- Bladder Cancer Advocacy Network (BCAN)minorTyra Biosciences and BCAN collaborated to establish May 21 as UTUC Awareness Day to promote awareness and research for upper tract urothelial carcinoma (UTUC), a rare cancer affecting the kidneys and ureters. Tyra is conducting clinical trials with dabogratinib, an FGFR3 inhibitor, for low-grade UTUC, aiming to develop kidney-sparing treatments.
- University of Kansas Medical CentercoreThe University of Kansas Medical Center is partnering with Tyra Biosciences on the SURF302 Phase 2 trial of dabogratinib (TYRA-300) in FGFR3-altered low-grade IR NMIBC, signaling external academic medical center confidence in Tyra's FGFR3-selective approach.
Scale indicators12 records
Recent moves1 record
Tyra Biosciences competitors and assessment
Company assessmentDirect peers
- QED Therapeutics (BridgeBio Pharma): QED Therapeutics, a BridgeBio affiliate, is developing infigratinib (FGFR1-3 inhibitor) across the same FGFR3-driven oncology indications and pediatric achondroplasia, making it the closest direct competitor to Tyra's dabogratinib across both oncology and skeletal dysplasia programs.
- Relay Therapeutics: Relay Therapeutics is a precision oncology company developing RLY-4008 (lirafugratinib), a selective FGFR2 inhibitor for FGFR2-altered cholangiocarcinoma and other solid tumors — directly comparable to Tyra's TYRA-200 in mechanism, target patient population, and selective-kinase-inhibitor strategy.
Broad incumbents
- Johnson & Johnson (Janssen): J&J's Janssen markets Balversa (erdafitinib), the first FGFR kinase inhibitor approved, including for FGFR3-altered NMIBC — directly overlapping Tyra's lead indication and raising the competitive bar Tyra must beat on selectivity and tolerability.
- Incyte Corporation: Incyte markets Pemazyre (pemigatinib), an FGFR1-3 inhibitor approved for FGFR2-altered cholangiocarcinoma, directly competing with Tyra's TYRA-200 and representing a commercial-stage incumbent that Tyra must displace or outflank.
- Taiho Pharmaceutical (Otsuka): Taiho markets Lytgobi (futibatinib), an irreversible FGFR1-4 inhibitor approved for FGFR2 fusion-positive cholangiocarcinoma and designed to address resistance mutations including gatekeeper variants — a direct mechanistic competitor to dabogratinib's V555 differentiation thesis.
- Blueprint Medicines (Sanofi): Blueprint Medicines, now part of Sanofi, develops precision oncology kinase inhibitors (Ayvakit for PDGFRA/GIST) and rare-disease therapies using structure-based design. Their successful commercial playbook in rare oncology and team hiring into Tyra (CRO Heather Faulds ex-Blueprint) make Blueprint a directly comparable model for go-to-market and pipeline strategy.
Emerging players
- Black Diamond Therapeutics: Black Diamond Therapeutics is a precision oncology company developing allosteric kinase inhibitors targeting oncogenic and resistance mutations, including in FGFR and other kinase families — sharing Tyra's strategy of designing against resistance mutations and structure-based inhibitor discovery.
- Cogent Biosciences: Cogent Biosciences is a clinical-stage precision oncology company developing selective kinase inhibitors (e.g., bezuclastinib for KIT-mutant GIST). It shares Tyra's model of structure-based, mutation-focused kinase-inhibitor development in oncology indications with limited treatment options.
Others
- Schrödinger, Inc. Schrödinger operates a computational drug discovery platform combining physics-based modeling with machine learning. While not a direct FGFR competitor, Schrödinger is highly comparable as a publicly traded platform-based drug discovery company using structural/precision methods to advance partnered and internal pipelines.
- Recursion Pharmaceuticals: Recursion is a clinical-stage AI-driven drug discovery company combining high-throughput biology with machine learning. While not kinase-focused, Recursion is comparable to Tyra as a publicly traded platform-enabled precision medicine company developing a multi-asset pipeline.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks7 records
Key highlights7 records
Customer concentration
Tyra Biosciences social profiles
Digital presenceTyra Biosciences compliance and trust
Trust signalCompliance1 record
Tyra Biosciences financial estimates
Financial estimateRevenue estimate
Valuation estimate
Tyra Biosciences leadership team
Management profileNumber of profiles
Profiles19 records
Tyra Biosciences funding detail
Funding detailFunding overview
Funding rounds5 records
Investors18 records
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Tyra Biosciences M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Tyra Biosciences
What does Tyra Biosciences do?
Tyra Biosciences is a clinical-stage biotechnology company that develops investigational, oral small-molecule precision medicines targeting fibroblast growth factor receptor (FGFR) biology for oncology and genetically defined conditions. The company is advancing three drug candidates — dabogratinib (FGFR3-selective), TYRA-430 (FGFR4/3-biased), and TYRA-200 (FGFR1/2/3) — designed using its proprietary SNAP Discovery Engine to overcome acquired resistance and improve isoform selectivity relative to first-generation FGFR inhibitors.
Is Tyra Biosciences a public or private company?
Tyra Biosciences is a public company. It is classified as public and is currently operating.
When was Tyra Biosciences founded?
Tyra Biosciences was founded in 2018. It employs 101 to 250 people.
Where is Tyra Biosciences based?
Tyra Biosciences is headquartered in Carlsbad, United States, in the North America region.
How does Tyra Biosciences make money?
Two revenue lines are on record. Pre-revenue clinical-stage pipeline is the primary driver. The others are capital markets financing (future R&D monetization).
Who are Tyra Biosciences's main competitors?
Direct peers on record are QED Therapeutics (BridgeBio Pharma) and Relay Therapeutics. Broad incumbents are Johnson & Johnson (Janssen), Incyte Corporation, Taiho Pharmaceutical (Otsuka) and Blueprint Medicines (Sanofi). Emerging players are Black Diamond Therapeutics and Cogent Biosciences. Others are Schrödinger, Inc. and Recursion Pharmaceuticals.
Does Tyra Biosciences have an API?
No public API is recorded for Tyra Biosciences.
What industry is Tyra Biosciences in?
Tyra Biosciences's product category is Precision Oncology Pharmaceuticals. Its primary akta.pro industry code is HLAIALAA, Drug Discovery (Target ID/Validation & Hit Discovery), with a secondary code of HLAIALAF, Translational Medicine & Biomarkers. Its NAICS code is 541714 and its SIC code is 2834.