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Tyra Biosciences, Inc. - TYRA STOCK NEWS

Welcome to our dedicated page for Tyra Biosciences news (Ticker: TYRA), a resource for investors and traders seeking the latest updates and insights on Tyra Biosciences stock.

Overview of Tyra Biosciences, Inc.

Tyra Biosciences, Inc. (Nasdaq: TYRA) is a clinical-stage biotechnology company dedicated to developing next-generation precision medicines. With a focus on precision oncology, FGFR biology, and targeted therapy, the company is pioneering treatments for challenging oncologic indications and genetically defined skeletal dysplasias. At its core, Tyra Biosciences leverages a proprietary drug discovery engine to tackle acquired resistance in cancer therapies and to address unmet medical needs in rare skeletal disorders.

Innovative SNÅP Platform

The foundation of Tyra Biosciences’ approach is its in-house precision medicine platform, SNÅP. This innovative technology allows for rapid and precise drug design through iterative molecular snapshots that accurately predict genetic alterations likely to drive resistance to existing treatments. The platform differentiates the company by enabling the development of drugs that are both highly specific and potentially better tolerated, addressing limitations associated with broader-spectrum FGFR inhibitors.

Clinical-Stage Pipeline and Core Programs

Tyra Biosciences has built a robust pipeline centered on its lead precision candidate, TYRA-300, an oral and highly selective FGFR3 inhibitor. Designed to avoid the toxicities often observed with pan-FGFR inhibition, TYRA-300 is under evaluation for multiple indications. In oncology, its application is primarily in advanced urothelial cancers characterized by FGFR3 gene alterations. Meanwhile, in the realm of skeletal dysplasias, TYRA-300 is being developed for conditions including achondroplasia and hypochondroplasia, with supportive preclinical data and regulatory designations that underscore its potential in addressing rare genetic disorders.

Therapeutic Focus and Market Position

Tyra Biosciences distinguishes itself within the competitive landscape through its targeted focus on FGFR-mediated diseases. By developing drugs that specifically target FGFR3 alterations, the company intends to overcome the frequently encountered challenges associated with acquired resistance. Its dual focus on oncology and rare skeletal dysplasias positions Tyra Biosciences in a unique niche, where precision medicine meets the imperative for improved tolerability and enhanced patient outcomes.

Research, Development, and Strategic Vision

The company’s strategy is built around its ability to translate cutting-edge scientific insight into therapeutic solutions. With an evolving portfolio of clinical-stage programs, Tyra Biosciences emphasizes iterative drug design, deep molecular understanding, and precision targeting. This meticulous approach not only paves the way for improved efficacy and safety profiles in its candidate drugs but also provides a flexible framework to address complex mutational landscapes in cancer and genetic disorders.

Operational Excellence and Future Relevance

Tyra Biosciences continues to advance its clinical programs through precise dose optimization, careful patient selection, and adherence to rigorous regulatory standards. The company’s development programs are structured on a sustainable, long-term basis, ensuring that the information provided remains relevant and evergreen. This emphasis on durable technological innovation and tactical execution underpins its commitment to scientific excellence and operational integrity.

Key Differentiators

  • Precision Platform: The SNÅP platform drives the rapid identification and development of targeted therapies.
  • Selective Inhibition: TYRA-300 is designed to selectively inhibit FGFR3, reducing off-target toxicities seen in pan-FGFR approaches.
  • Diverse Pipeline: The development programs cover both oncology and rare skeletal dysplasias, addressing significant unmet clinical needs.
  • Innovative Drug Design: Iterative molecular snapshots enhance the precision of drug design, allowing the tailoring of therapies to specific genetic profiles.

Conclusion

In summary, Tyra Biosciences, Inc. stands at the forefront of precision medicine with its innovative SNÅP platform and a strategic focus on FGFR biology. Its clinical-stage pipeline, led by TYRA-300, exemplifies the company’s commitment to developing targeted therapies that promise improved efficacy and tolerability for conditions with unmet medical needs. Through precise and iterative drug development, Tyra Biosciences is poised to be an informative case study in how targeted molecular strategies can redefine therapeutic approaches in both oncology and rare genetic disorders.

Rhea-AI Summary
Tyra Biosciences, Inc. has received Orphan Drug Designation from the FDA for its lead precision medicine program, TYRA-300, for the treatment of achondroplasia, the most common form of dwarfism. TYRA-300 is an oral FGFR3 selective inhibitor that aims to address height and long-term health complications associated with achondroplasia. The company plans to submit an IND to the FDA for a Phase 2 study in pediatric achondroplasia in 2024.
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Tyra Biosciences (Nasdaq: TYRA), a clinical-stage biotechnology firm, announced its participation in key investor conferences. CEO Todd Harris will engage in a fireside chat at Cantor's The Future of Oncology Virtual Symposium on April 4, 2023, at 2:15 PM ET. He will also present at the Bank of America 2023 Healthcare Conference on May 11, 2023, at 9:35 AM PT. TYRA focuses on developing precision medicines targeting FGFR biology and utilizes its innovative SNÅP platform for drug design. For live updates and webcasts, visit the company's investor page.

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Tyra Biosciences (TYRA) reported financial results for 2022 and highlighted key milestones. The company initiated patient dosing for TYRA-300 in the SURF301 oncology study and expanded its pipeline to treat achondroplasia. The FDA cleared the IND for TYRA-200's Phase 1 study, expected to begin in 2H 2023. For 2022, TYRA recorded a full-year net loss of $55.3 million, compared to $26.3 million in 2021. R&D expenses increased to $43 million, and the company maintains a strong cash position with $251.2 million available, ensuring over two years of runway for its development plans.

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Tyra Biosciences (Nasdaq: TYRA) announced the expansion of TYRA-300's development into achondroplasia following promising preclinical results. The oral FGFR3 selective inhibitor exhibited significant growth and bone length increases in preclinical models, including a 17.6% increase in body length and notable femur and tibia length improvements. A Phase 2 clinical study is planned for 2024, addressing unmet medical needs in children with achondroplasia. Additionally, TYRA has received FDA clearance for a Phase 1 study of TYRA-200, aimed at advancing its pipeline. A conference call was held on March 1 to discuss these developments.

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Tyra Biosciences (Nasdaq: TYRA), a precision oncology company, announced its participation in two upcoming investor conferences. CEO Todd Harris will engage in a fireside chat at the Cowen 43rd Annual Healthcare Conference on March 7, 2023, at 10:30 am ET. Additionally, he will provide a company overview virtually at the Oppenheimer 33rd Annual Healthcare Conference on March 15, 2023, at 12:00 pm ET. Live and archived webcasts can be accessed through the Investor section of the TYRA website. Tyra focuses on developing therapies to combat tumor resistance, utilizing its proprietary SNÅP platform to design selective inhibitors targeting FGFR.

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Tyra Biosciences has initiated the SURF301 Phase 1/2 clinical study for TYRA-300, an oral FGFR3-selective inhibitor for metastatic urothelial carcinoma, marking a pivotal shift to a clinical-stage company. The first patient has been dosed, with an emphasis on addressing unmet needs in both FGFR resistant and naïve populations. The study aims to establish optimal dosing and evaluate preliminary antitumor activity. Results and updates will be shared as data matures, with further details available on their website.

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Tyra Biosciences (Nasdaq: TYRA) announced its participation in key investor conferences on November 14 and 15-17, 2022. CEO Todd Harris will engage in fireside chats at both events, aiming to showcase the company's innovations in precision oncology. The H.C. Wainwright 3rd Annual Precision Oncology Virtual Conference will feature a chat available on demand, while the Jefferies London Healthcare Conference will include a live chat on November 15 at 10:50 am ET. Webcasts of these discussions will be accessible on the TYRA Investor section.

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Tyra Biosciences, Inc. (TYRA) reported its third-quarter 2022 financial results, highlighting a net loss of $12.5 million, an increase from $6.6 million in Q3 2021. Research and development expenses rose to $10.9 million, compared to $5.5 million in the prior year. As of September 30, 2022, cash and cash equivalents stood at $263.2 million. The company is focused on advancing its pipeline, which includes the initiation of the SURF301 study for TYRA-300 and filing an IND for TYRA-200 by year-end 2022.

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FAQ

What is the current stock price of Tyra Biosciences (TYRA)?

The current stock price of Tyra Biosciences (TYRA) is $8.72 as of April 1, 2025.

What is the market cap of Tyra Biosciences (TYRA)?

The market cap of Tyra Biosciences (TYRA) is approximately 462.9M.

What is the core focus of Tyra Biosciences?

Tyra Biosciences is focused on developing next-generation precision medicines targeting aberrations in FGFR biology. It primarily addresses unmet needs in oncology and rare skeletal dysplasias.

How does the SNÅP platform contribute to the company’s drug development?

The SNÅP platform enables rapid and precise drug design by using iterative molecular snapshots to predict genetic alterations. This facilitates the creation of highly selective therapies with potentially improved tolerability.

What is TYRA-300 and in which indications is it being evaluated?

TYRA-300 is an investigational, oral, FGFR3-selective inhibitor developed for the treatment of cancer and skeletal dysplasias. It is currently being evaluated in clinical studies for advanced urothelial carcinoma and conditions such as achondroplasia and hypochondroplasia.

How does Tyra Biosciences address the issue of acquired resistance in cancer therapies?

By leveraging its SNÅP platform, the company designs precision medicines that specifically target genetic mutations responsible for acquired resistance. This focused approach aims to enhance the efficacy and safety profile of its treatments compared to broader-acting therapies.

What sets Tyra Biosciences apart from other biotechnology companies?

The company distinguishes itself through its proprietary SNÅP platform and a focused development program targeting FGFR-mediated diseases. This specialized approach enables the design of highly selective drugs that aim to reduce on-target toxicities and overcome resistance challenges.

What are the strategic benefits of developing therapies for both oncology and skeletal dysplasias?

Targeting both oncology and skeletal dysplasias allows Tyra Biosciences to address significant unmet medical needs across diverse patient populations. This dual focus leverages common genetic targets and maximizes the utility of its precision medicine platform.

How does Tyra Biosciences ensure the durability and relevance of its clinical programs?

The company designs its clinical programs with a long-term perspective, emphasizing iterative drug development and precise targeting of genetic alterations. This approach, coupled with comprehensive preclinical and clinical evaluation, ensures the information remains evergreen and relevant.

What common challenges in drug development does Tyra Biosciences aim to overcome?

Tyra Biosciences aims to overcome challenges such as acquired resistance to existing therapies and the toxicities associated with pan-FGFR inhibitors. Their approach focuses on developing selective therapies that enhance treatment tolerability and efficacy.
Tyra Biosciences, Inc.

Nasdaq:TYRA

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462.94M
49.40M
4.64%
100.46%
8.06%
Biotechnology
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