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Relay Therapeutics uses its Dynamo platform to discover drugs by exploring how proteins move, enabling them to target proteins previously considered undruggable. The platform blends experimental data with computational modeling to identify and optimize therapeutic candidates, with a focus on precision oncology and genetic diseases. Its approach combines motion biology, data-driven design, and active partnerships (such as a worldwide license and collaboration with Genentech) with an internal drug pipeline. The company aims to bring life-changing medicines to patients by advancing clinical trials and securing licensing collaborations to fund and validate its therapies.
Industries
AI & Machine Learning
Biotechnology
Healthcare
Company Size
201-500
Company Stage
IPO
Headquarters
Cambridge, Massachusetts
Founded
2016
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Relay Therapeutics shares surge 20% on ASCO momentum for zovegalisib breast cancer program. Relay Therapeutics gains investor interest with promising data on its lead cancer therapy at ASCO 2026. Published 06/03/26 AT 12:16 AM AEST NEW YORK - Relay Therapeutics Inc. shares climbed more than 20% in morning trading Tuesday, reaching $17.12 as investors responded to ongoing buzz around the company's precision oncology pipeline at the American Society of Clinical Oncology annual meeting in Chicago. The clinical-stage biotechnology company, focused on small molecule therapies for cancer and genetic diseases, has seen renewed interest in its lead candidate zovegalisib (RLY-2608), a mutant-selective PI3Kα inhibitor. The stock's sharp move comes amid broader sector enthusiasm for oncology advancements showcased at the May 29-June 2 gathering. Zovegalisib continues to generate attention following earlier data readouts demonstrating clinically meaningful progression-free survival in PIK3CA-mutated, HR+/HER2- metastatic breast cancer. The program holds FDA Breakthrough Therapy designation, signaling regulatory recognition of its potential. Clinical Progress on Zovegalisib Updated interim results from the Phase 1/2 ReDiscover trial previously showed a median progression-free survival of 11.0 months in second-line patients treated with zovegalisib plus fulvestrant. Objective response rates reached 39% overall in patients with measurable disease, with consistent efficacy observed across kinase and non-kinase PIK3CA mutations. These findings, initially highlighted at prior scientific meetings, underscore zovegalisib's differentiated profile compared to non-selective PI3K inhibitors, which have faced challenges with toxicity such as hyperglycemia. The ongoing Phase 3 ReDiscover-2 trial evaluates the combination in CDK4/6-experienced patients. At ASCO 2026, Relay's presence contributes to the narrative of advancing targeted therapies in areas with significant unmet need. Approximately 40% of HR+/HER2- advanced breast cancer patients harbor PIK3CA mutations, often facing limited options after CDK4/6 inhibitor progression. Pipeline Expansion and Additional Data Beyond breast cancer, Relay has advanced zovegalisib into PIK3CA-driven vascular anomalies. Initial Phase 2 ReInspire trial results presented earlier highlighted encouraging safety and efficacy signals in this rare disease setting. The company's Dynamo platform, which integrates computational and experimental approaches to target protein motion, underpins its discovery efforts. This technology aims to address previously intractable targets through allosteric modulation. Relay also maintains a broader pipeline, including earlier-stage programs in oncology and genetic diseases, though zovegalisib remains the primary value driver. Financial Position Strengthened Relay reported $642.1 million in cash, cash equivalents and investments as of March 31, 2026, up from $554.5 million at year-end 2025. The increase followed net proceeds from at-the-market offerings. A subsequent May public offering added approximately $296.8 million in net proceeds. Management has stated that current resources provide runway into 2029, supporting continued clinical execution. First-quarter 2026 revenue was $3.0 million, primarily from a licensing agreement, with a net loss of $73.3 million. Analyst and Market Sentiment Wall Street maintains a generally positive stance on Relay, with consensus price targets around $21-$23. Ratings lean toward buy, reflecting optimism around zovegalisib's potential in a large addressable market. The stock's recent volatility aligns with typical biotech patterns tied to clinical catalysts. Tuesday's volume spike reflects heightened investor interest amid ASCO presentations across the oncology sector. Challenges and Competitive Landscape The PI3Kα space remains competitive, with other agents like capivasertib approved in similar settings. Relay's mutant-selective approach seeks to offer improved tolerability while maintaining efficacy, a key differentiator if Phase 3 data confirm earlier signals. Risks include clinical execution, regulatory outcomes, manufacturing scalability and broader biotech funding dynamics. Any data readouts showing efficacy compression or unexpected toxicities could pressure the stock. Broader Industry Context ASCO 2026 has featured multiple advances in targeted therapies and combination approaches for lung cancer, sarcoma and other malignancies. Positive momentum across oncology names has supported sector sentiment despite macroeconomic uncertainties. Relay's strategy positions it at the intersection of precision medicine and computational drug design. Success with zovegalisib could validate the platform and open opportunities for additional programs. Investment Considerations At current levels near $17, Relay trades with elevated expectations for its lead asset. The company's cash position provides flexibility for business development or accelerated development timelines. However, as a pre-commercial entity, it carries typical biotech risks including binary clinical outcomes. Financial advisors recommend careful position sizing given volatility. Diversification across the sector and attention to upcoming milestones, including potential conference updates and Phase 3 progress, remain important. Management will participate in upcoming investor conferences, including the Jefferies Global Healthcare Conference on June 3 and Goldman Sachs on June 8, providing further opportunities to discuss strategy. Relay Therapeutics enters the second half of 2026 with key data catalysts and a strengthened balance sheet. Whether Tuesday's gains hold will depend on sustained positive sentiment from ASCO, execution on the zovegalisib program and broader market conditions. The company's focus on transforming drug discovery through motion-based insights offers a compelling long-term narrative. As clinical programs mature, Relay could emerge as a significant player in precision oncology if it delivers on its pipeline promise. MEET IBT NEWS FROM BELOW CHANNELS
Relay Therapeutics, a clinical-stage precision medicine company, has priced an underwritten public offering of 22,916,667 shares at $12 per share. Underwriters exercised their full option to purchase an additional 3,437,500 shares, bringing gross proceeds to approximately $316 million before deducting fees and expenses. The company develops small molecule therapies for cancer and genetic diseases using its Dynamo platform. Its lead asset, zovegalisib, is the first pan-mutant selective PI3Kα inhibitor in clinical development, currently in a Phase 3 trial for metastatic breast cancer. The drug is also being studied for genetic vascular anomalies. Goodwin's Life Sciences team advised on the transaction, led by Gabriela Morales-Rivera, Kristin Yeakel, Megan Riley, Caleb Paasche and Bill Collins.
Relay doubles the bar, outpacing Novartis with a 60% response in rare disease. Posted on May 20, 2026 By News Team Analysts are extremely encouraged by Phase 2 trial results for Relay Therapeutics' PI3KA inhibitor in treating vascular malformations (VM), prompting the biotech to eye a potential path to accelerated approval. Relay's investigational PI3KA inhibitor has elicited a 60% response rate in patients with vascular malformations, toppling Novartis' 11% overall response rate seen in a failed Phase 2 study of Vijoice. The biotech's execs are now looking to the FDA's accelerated approval pathway for the oral PI3KA inhibitor, called zovegalisib, pending additional data and feedback from regulators. The early-stage data include adults and children older than 12 years with vascular anomalies - an umbrella term for rare disorders marked by abnormal development of blood vessels, lymphatic vessels and nearby tissues. As of April 15, 32 patients were enrolled in the Phase 2 ReInspire trial, of which 22 patients had PIK3Ca-related overgrowth spectrum (PROS) - disorders caused by mutations in the PI3Ka gene. Of 20 evaluable patients, 12 - or 60% - achieved a volumetric response at 12 weeks, according to data set for presentation Wednesday at the International Society for the Study of Vascular Anomalies World Congress 2026. The overall response rate (ORR) doubles Leerink Partners' "prior bar for success" of 20%-25% ORR and is higher than the 11% ORR seen at week 16 for Novartis' oral PI3K inhibitor Vijoice in a failed PROS study. After Relay's data cutoff of April 15, one additional patient had an unconfirmed response, resulting in a 65% (13/20) ORR, according to the Cambridge, Massachusetts-based biotech. The data show "the full potential of what a mutant selective inhibitor can do in these vascular anomaly patients," Relay CEO Sanjiv Patel said on a Tuesday conference call. "[We] believe this leaves very little room for improvement of our volumetric response rate for anyone that will come behind us." At 12 weeks, interim investigator-measured impressions of change showed 89% of patients experiencing clinical improvement, while patient reports for the same metric were 79%. Pain scores, as measured by investigators, demonstrated clinical improvement for 71% of symptoms. "Given these superlative results, we think it is possible RLAY shares could exceed our anticipated >10% move as some investors may adopt VM as the main value driver," Leerink said. Since market open, the biotech's stock has risen 9% to $13.29 per share. The trial is testing doses of 100 mg, 300 mg and 400 mg twice daily. "We believe there is no further efficacy left on the table," Patel said about the 300-mg dosing regimen. "As you go above that, you're just seeing greater tolerability challenges, and so we don't think there's any room for us to go higher than 300." The rates of treatment-related adverse events (TRAEs) among 22 patients were "proportional to dose level," with no dose discontinuations, according to Relay. Two patients (9%) experienced a grade 3 or higher TRAE. Zovegalisib wasn't tied to rashes or stomatitis of any grade, and no cases of grade 3 or higher hyperglycemia or diarrhea were reported, though the biotech did not disclose all the data for adverse events. Overall, zovegalisib's tolerability profile was generally "as expected and consistent with mutant-selective PI3Kα inhibition," according to Relay. The rates of key adverse events such as hyperglycemia, stomatitis and rash were lower than or similar to Vijoice, according to Leerink. Based on the newest findings, Relay is opening multiple expansion cohorts at 400 mg once a day and 300 mg twice daily in patients 12 years and older, with a dose-finding trial for patients aged six to 11 years ongoing. Zovegalisib is also in later-stage testing for multiple metastatic breast cancers.
Relay Therapeutics missed first-quarter earnings expectations, with revenues of $3.0 million falling 35% short of forecasts and statutory losses of $0.41 per share exceeding estimates by 15%. Following the results, seven analysts cut their revenue forecasts for 2026 to $8.54 million, representing a 20% year-on-year decline, down from previous expectations of $9.68 million. Loss per share estimates increased slightly to $1.55 from $1.51. Despite the weaker outlook, the average price target rose 17% to $21.00, suggesting confidence in longer-term performance. Analyst valuations range from $18.00 to $25.00 per share. The forecast 26% annualised revenue decline compares unfavourably to the broader industry's expected 21% annual growth, though it represents an improvement on Relay Therapeutics' historical 39% annual revenue shrinkage over the past five years.
Relay Therapeutics plans to advance zovegalisib into Phase 3 development for frontline PI3Ka mutated HR+/HER2- metastatic breast cancer, based on encouraging efficacy data and a manageable safety profile in heavily pre-treated patients. Zovegalisib is an allosteric, pan-mutant, isoform-selective PI3Ka inhibitor developed using the company's proprietary precision oncology platform. The advancement targets a large breast cancer patient group with limited treatment options for PI3Ka mutations. The company's shares currently trade at $12.72, approximately 39% below the analyst consensus target of $21.00. Relay Therapeutics remains loss-making, reporting net losses of $276.5 million. Investors will be watching for Phase 3 trial design details and regulatory interactions as key indicators of the programme's commercial potential.
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Industries
AI & Machine Learning
Biotechnology
Healthcare
Company Size
201-500
Company Stage
IPO
Headquarters
Cambridge, Massachusetts
Founded
2016
Find jobs on Simplify and start your career today