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Tyra Biosciences

Develops precision oncology therapies targeting FGFR

Overview

Tyra Biosciences develops precision medicines for cancer and genetically defined diseases using its SNAP platform to target specific genetic mutations. Its lead programs include TYRA-300, an FGFR3 inhibitor for achondroplasia and non-muscle invasive bladder cancer, and TYRA-200, an FGFR1/2/3 inhibitor for intrahepatic cholangiocarcinoma and other solid tumors. The SNAP platform supports mutation-focused drug design to overcome resistance and tailor therapies, aided by collaborations with academic partners to advance trials. Funding comes from venture capital and public offerings, with future revenue expected from drug sales and licensing upon regulatory approval, and the goal of bringing targeted, effective treatments to patients by moving candidates through clinical development toward commercialization.

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About Tyra Biosciences

Simplify's Rating
Why Tyra Biosciences is rated
B-
Rated B on Competitive Edge
Rated B on Growth Potential
Rated C on Differentiation

Industries

BiotechnologyHealthcare

Company Size

51-200

Company Stage

IPO

Headquarters

Carlsbad, CA

Founded

2018

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What believers are saying

  • September 2026 financing and $700.5 million cash fund operations through 2030.
  • SURF302 showed no Grade 3 treatment-related adverse events at 60 mg and favorable tolerability.
  • BEACH301 and SURF303 each have 2027 readouts, creating multiple near-term catalysts.

What critics are saying

  • SURF302 disappointed investors on September 9, 2026, triggering a 17.66% stock drop and investigations.
  • Tyra reported no material legal proceedings, yet Pomerantz and Bronstein launched securities probes.
  • Achondroplasia and urothelial programs remain precommercial; one failed Phase 3 would crush TYRA.

What makes Tyra Biosciences unique

  • Dabogratinib showed 79% ORR in SURF302 on September 9, 2026, with 60 mg dosing.
  • Tyra owns a selective FGFR3 strategy targeting bladder cancer and achondroplasia, not broad oncology.
  • SNÅP platform supports rapid FGFR drug design and iterative optimization across mutation-specific programs.

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Funding

Total Funding

$955M

Above

Industry Average

Funded Over

5 Rounds

Post IPO Equity funding comparison data is currently unavailable. We're working to provide this information soon!
Post IPO Equity Funding Comparison Coming Soon

Benefits

  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Life Insurance
  • Disability Insurance
  • 401(k) Company Match
  • Employee Stock Purchase Plan
  • Paid Holidays
  • Paid Sick Leave
  • Paid Parental Leave
  • Tuition Reimbursement
  • Wellness Program

Stock Price

Company News

Securities.io
Nov 10th, 2026
Tyra Biosciences Q3 loss widens to $51.1 million as research costs rise.

Tyra Biosciences Q3 loss widens to $51.1 million as research costs rise. Published November 10, 2026 Louis Mbaye Pharma & AI Drug Discovery, AI Research Agent On November 10, 2026, Tyra Biosciences reported third-quarter results showing a $51.1 million net loss for the quarter ended September 30, 2026, compared with $29.9 million in the same period of 2025, as spending increased on three clinical programs for its lead drug candidate, dabogratinib. The clinical-stage company ended the quarter with $700.5 million in cash, cash equivalents and marketable securities following a September financing, and expects its current resources to fund planned operations through 2030. Research spending drives the wider loss. Research and development expense rose to $43.1 million from $25.5 million. Tyra attributed the increase primarily to dabogratinib development across SURF303, SURF302 and BEACH301, with higher personnel, facilities and other costs also contributing as clinical and development activities expanded. General and administrative expense increased to $11.7 million from $7.5 million, primarily because of compensation and other personnel costs tied to headcount growth. Together, the two expense lines show that both trial activity and organizational growth contributed to the loss. September financing extends funding horizon. An underwritten public offering of common stock and pre-funded warrants, completed in September 2026, generated approximately $400 million in gross proceeds before underwriting discounts, commissions and offering expenses. RA Capital Management led the financing, which was priced on September 14, 2026. Tyra said net proceeds and existing liquidity would support the three-program dabogratinib strategy, preclinical and discovery work, working capital and general corporate purposes. The raise provides a multi-year funding horizon as the company prepares for regulatory discussions and potential Phase 3 development. Earlier SURF302 results frame Phase 3 plans. Clinical results included in the quarterly update were first announced on September 9, 2026, with an August 31, 2026 data cutoff. In the Phase 2 SURF302 study of FGFR3-altered low-grade intermediate-risk non-muscle invasive bladder cancer, Tyra reported that 60 mg once daily produced a 79% overall response rate (11 of 14 participants) and a 64% best-overall-response complete-response rate (9 of 14) across single and multiple marker lesions. Among eight participants with a single marker lesion, those rates were 100% and 75%, respectively. All responses remained subject to change with continued treatment and follow-up. Across 44 participants in the 50 mg and 60 mg safety cohorts, Tyra reported no Grade 4 or 5 treatment-emergent adverse events and two Grade 3 treatment-related adverse events, both at 50 mg. No clinically significant hyperphosphatemia, nail toxicity or ocular toxicity was observed. Enrollment in the 60 mg cohort is complete, and a 70 mg cohort is enrolling to explore the ablative setting further. Tyra expects to initiate a Phase 3 adjuvant study in 2027, subject to regulatory feedback. Other programs approach 2027 readouts. SURF303 is a multicenter, open-label Phase 2a/b study designed with pivotal intent to evaluate 60 mg and 80 mg once-daily doses in low-grade upper tract urothelial carcinoma. Tyra reported a three-month complete response in its first treated participant on 60 mg, with no observed treatment-emergent adverse events as of August 31, and expects additional results in 2027. That single-patient observation was also first reported in September 2026. BEACH301 is evaluating children ages 3 to 10 with achondroplasia. After five safety-sentinel dose levels, the Data Safety Monitoring Committee authorized a sixth at 0.875 mg/kg. Tyra expects initial results from approximately 25 children in 2027, including six-month annualized height velocity and safety data. The quarter ties a widening loss to a broader clinical workload, while the September financing supplies capital for the next stage. The central question for 2027 is whether additional SURF302 data and regulatory feedback support the planned Phase 3 adjuvant study, while further SURF303 observations and the first BEACH301 sentinel results clarify the evidence across Tyra's three-program strategy. Louis Mbaye is an AI-generated markets research agent at Securities.io, covering Pharma & AI Drug Discovery and the public companies, market infrastructure and investable technologies shaping that field. Louis Mbaye monitors pharmaceutical pipelines, AI drug discovery, trial readouts, approvals, licensing, patent events, manufacturing and material biotech M&A. Coverage follows a clinical, pipeline-focused, methodical perspective, prioritizing first-party announcements, company fundamentals, competitive positioning and developments with material relevance for investors. Articles authored by Louis Mbaye are AI-generated and reviewed by Securities.io's editorial team to ensure factual accuracy, source quality and responsible coverage. Content is provided for educational purposes and does not constitute investment advice.

DirectorsTalk Interviews
Oct 2nd, 2026
Tyra Biosciences, Inc. (TYRA) stock analysis: exploring a potential 125% upside in the biotech arena.

Tyra Biosciences, Inc. (TYRA) stock analysis: exploring a potential 125% upside in the biotech arena. Tyra Biosciences, Inc. (NASDAQ: TYRA), a clinical-stage biotechnology firm, is making waves in the healthcare sector with its innovative approach to developing precision medicines targeting fibroblast growth factor receptor (FGFR) biology. Positioned at the cutting edge of biotechnology, Tyra Biosciences is engaging the market with a strong focus on oncology and genetically defined conditions. With a market capitalization of $1.44 billion, this Carlsbad, California-based company is worth a closer look for investors seeking high-risk, high-reward opportunities. Currently trading at $21.01, Tyra Biosciences' stock has experienced a dip, marked by a recent price change of -0.86 (-0.04%). Despite this minor setback, the company has shown resilience within a 52-week range of $13.37 to $39.61, indicating significant volatility that could spell opportunity for savvy investors. Notably, the company's average target price stands at $47.45, suggesting a potential upside of 125.87% from its current price point. Tyra Biosciences is not yet profitable, as evidenced by its trailing P/E ratio and PEG ratio both being unavailable and a forward P/E ratio of -7.58. This negative forward P/E suggests that the company is still in its growth phase, reinvesting heavily in research and development rather than generating positive earnings. The company's return on equity is a concerning -45.31%, and it reports an EPS of -2.30, emphasizing the challenges it faces in achieving profitability. The negative free cash flow of $63,067,124 further underscores the company's current focus on expansion and development over immediate profitability. Despite these financial hurdles, the market sentiment towards Tyra Biosciences remains overwhelmingly positive. Out of 15 analyst ratings, 14 rate it as a "Buy" while only one suggests a "Hold," and none recommend selling. This strong endorsement from analysts is likely driven by the company's promising pipeline of product candidates. Tyra's SNÅP platform, which facilitates precision drug design, and its leading product candidate FGFR3, targeting metastatic urothelial carcinoma and other solid tumors, are at the forefront of its clinical pursuits. Additionally, the company is developing TYRA-300 for skeletal conditions and TYRA-200 and TYRA-430 for various forms of cancer, all of which highlight the breadth of its innovative capabilities. From a technical perspective, Tyra Biosciences' stock indicates some consolidation. The 50-day moving average of $26.09 and the 200-day moving average of $30.52 suggest that the stock is currently trading below both averages, potentially representing a buying opportunity for investors who believe in the company's long-term potential. The Relative Strength Index (RSI) of 54.75 indicates a relatively neutral position, neither overbought nor oversold. For investors with a high-risk tolerance, Tyra Biosciences presents an intriguing opportunity. The company's focus on revolutionary treatments for serious health conditions, coupled with a robust pipeline and strong analyst support, positions it as a potential winner in the biotech sector. However, prospective investors should be mindful of the inherent risks associated with investing in clinical-stage biotech firms, including the uncertainty of clinical trials and regulatory approvals. Tyra Biosciences, Inc. is at a pivotal point in its journey, making now an exciting time to consider this stock for those willing to navigate the volatility of the biotech industry. With a promising future ahead, the potential rewards could be significant for investors who align with the company's vision and are prepared for its financial ebbs and flows. * Written by: Madison Wilson

GlobeNewswire
Sep 15th, 2026
INVESTOR ALERT: Pomerantz law Firm investigates claims on behalf of investors of Tyra Biosciences, Inc. - TYRA.

INVESTOR ALERT: Pomerantz law Firm investigates claims on behalf of investors of Tyra Biosciences, Inc. - TYRA. September 15, 2026 17:32 ET | Source: Pomerantz LLP NEW YORK, Sept. 15, 2026 (GLOBE NEWSWIRE) - Pomerantz LLP is investigating claims on behalf of investors of Tyra Biosciences, Inc. ("Tyra" or the "Company") (NASDAQ: TYRA). Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext. 7980. The investigation concerns whether Tyra and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. On September 9, 2026, Tyra issued a press release "announc[ing] initial results from SURF302, its Phase 2 study evaluating oral dabogratinib in patients with FGFR3-altered low-grade intermediate-risk non-muscle invasive bladder cancer (LG IR NMIBC)." While the Company said that the data indicated a favorable safety profile, 14% and 9% of participants in the 60 mg once-daily ("QD") and 50 mg QD dose cohorts experienced Grade 3 treatment-emergent adverse events. On this news, Tyra's stock price fell $4.72 per share, or 17.66%, to close at $22.01 per share on September 9, 2026. Pomerantz LLP, with offices in New York, Chicago, Los Angeles, London, Paris, and Tel Aviv, is acknowledged as one of the premier firms in the areas of corporate, securities, and antitrust class litigation. Founded by the late Abraham L. Pomerantz, known as the dean of the class action bar, Pomerantz pioneered the field of securities class actions. Today, more than 85 years later, Pomerantz continues in the tradition he established, fighting for the rights of the victims of securities fraud, breaches of fiduciary duty, and corporate misconduct. The Firm has recovered numerous multimillion-dollar damages awards on behalf of class members. See www.pomlaw.com. Attorney advertising. Prior results do not guarantee similar outcomes.

Morningstar
Sep 14th, 2026
Tyra Biosciences prices $400M stock offering to advance FGFR-targeted cancer therapies

Tyra Biosciences has priced a $400 million underwritten offering of common stock and pre-funded warrants. The clinical-stage biotechnology company will sell 9,079,000 shares at $22.03 per share and pre-funded warrants to purchase 9,078,529 shares at $22.029 per share. The offering is expected to close on 15 September 2026. Tyra plans to use the net proceeds to advance its "dabogratinib 3x3" development strategy in low-grade upper tract urothelial carcinoma, intermediate-risk non-muscle invasive bladder cancer, and achondroplasia, alongside supporting preclinical programmes. RA Capital Management led the offering, with participation from new and existing institutional investors including Invus, Commodore Capital, and Janus Henderson Investors. Jefferies, Guggenheim Securities, Cantor, Barclays, and William Blair are acting as joint book-running managers.

BioSpace
Sep 10th, 2026
Tyra shares slip as bladder cancer responses fall short of investor expectations.

Tyra shares slip as bladder cancer responses fall short of investor expectations. September 10, 2026 | Despite falling short of analyst expectations, Tyra Biosciences is taking its cancer drug to registrational development for non-muscle invasive bladder cancer. Response rates for Tyra Biosciences' investigational bladder cancer pill came in below investor expectations, dragging the biotech's shares down nearly 18%. Tyra is testing the drug candidate, dubbed dabogratinib, in the Phase 2 SURF302 study, focusing on patients with low-grade intermediate-risk non-muscle invasive bladder cancer. Initial results, presented Wednesday, showed that eight of 14 patients had no detectable signs of cancer at the three-month assessment, yielding a complete response (CR) rate of 57%. This was the primary goal of the study. Meanwhile, overall response rate was 79%, while partial response was 21%. Dabogratinib's 57% CR came below analyst expectations. William Blair, for instance, had been anticipating CR rates between 70% to 80%. Investors appear to have also been looking forward to stronger results: shares of the California company dropped 17.66% to $22.01 at market close Wednesday. As for safety, Tyra documented two patients who developed grade 3 treatment-related adverse events, resulting in a 9% incidence rate. There were no grade 4 or 5 events reported. William Blair called dabogratinib's safety profile "highly favorable," contending that it "continues to support the core differentiation thesis" for the asset. Despite the underwhelming readout, Tyra has decided to push dabogratinib into registrational development - a move that William Blair is supportive of. "We continue to believe the dataset supports advancement into adjuvant Phase 3 development and preserves a viable path to generating clinically meaningful disease-free survival benefit," the firm said in a Wednesday note, however conceding that SURF302's readout was "more nuanced than anticipated" and will "likely require investors to recalibrate expectations." Bristol Myers Squibb is positioning arlo-cel for quadruple-class exposed patients, which could help reduce competition with an upcoming multiple myeloma CAR T therapy from Gilead Sciences, according to BMO Capital Markets. September 9, 2026 In particular, the analysts pointed out that response rates to dabogratinib "appeared heavily influenced by residual marker lesion burden," or how much cancer is left behind after initial treatment. Indeed, CR increased to 63% in patients with single marker lesions - a residual burden that according to Tyra Chief Medical Officer Doug Warner "most closely mirrors the adjuvant setting," where no tumor remains. The biotech plans to design dabogratinib's late-stage program in the adjuvant setting. Taken orally, dabogratinib is a precision medicine that targets and inhibits the FGFR3 protein, which plays a crucial role in regulating cell development, growth and division. Unlike currently available FGFR3 inhibitors, dabogratinib is designed to address emerging treatment resistance and to be more selective for FGFR3 than other forms of the FGFR protein, in turn limiting off-target effects, Tyra claims on its website. Aside from non-muscle invasive bladder cancer, the company is also studying dabogratinib for low-grade upper tract urothelial cancer, for which the Phase 2 SURF303 trial is ongoing. The first patient dosed in the study showed a complete response at three months, Tyra said on Wednesday. Dabogratinib is also being tested for skeletal dysplasias, including achondroplasia. Tristan is BioSpace 's senior staff writer. Based in Metro Manila, Tristan has more than eight years of experience writing about medicine, biotech and science. He can be reached at [email protected], [email protected] or on LinkedIn.

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