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Relay Therapeutics, Inc. develops clinical-stage small molecule precision medicines for cancer and genetic disease. The company uses its Dynamo® platform, which combines computational and experimental approaches to drug protein targets that have been intractable or inadequately addressed.
Recurring RLAY news centers on zovegalisib (RLY-2608), a mutant-selective PI3Kα inhibitor studied in HR+/HER2- metastatic breast cancer and PI3Kα-driven vascular anomalies. Company updates also cover pipeline programs for NRAS-driven solid tumors and Fabry disease, clinical and regulatory data presentations, operating results, capital-structure matters, license or collaboration agreements, and governance developments.
Relay Therapeutics (Nasdaq: RLAY) announced that management will participate in two investor fireside chats in June 2026.
Events include the 2026 Jefferies Global Healthcare Conference on June 3 at 12:45 p.m. ET and the Goldman Sachs 47th Annual Global Healthcare Conference on June 8 at 8:40 a.m. ET. Both will be webcast live, with replays available for 30 days.
Relay Therapeutics (Nasdaq: RLAY) priced an underwritten public offering of 22,916,667 common shares at $12.00 per share. Underwriters have a 30-day option to buy up to 3,437,500 additional shares.
Gross proceeds are expected to be about $275 million, before fees, with closing expected on or about May 22, 2026, subject to customary conditions.
Relay Therapeutics (Nasdaq: RLAY) has launched an underwritten public offering of $175 million of common stock. The company plans to grant underwriters a 30-day option to buy up to an additional 15% of the shares.
All shares are to be sold by Relay Therapeutics under an effective Form S-3ASR shelf registration. Jefferies, TD Cowen, Goldman Sachs and Guggenheim Securities are joint bookrunners, with Raymond James as lead manager. The deal’s timing, size and terms remain subject to market conditions.
Relay Therapeutics (Nasdaq: RLAY) reported initial Phase 2 ReInspire data for zovegalisib in PIK3CA-driven vascular anomalies. Among 20 response-evaluable adults/adolescents, 60% showed volumetric lesion response at 12 weeks, rising to 65% after data cut-off, with 89% investigator- and 79% patient-reported clinical improvement and an interim safety profile supporting chronic dosing at optimized regimens.
Relay Therapeutics (Nasdaq: RLAY) reported Q1 2026 results and program updates on May 5, 2026. Key items: FDA Breakthrough Therapy designation for zovegalisib in PIK3CA‑mutant HR+/HER2‑ advanced breast cancer; 11.1‑month median PFS in CDK4/6‑experienced patients; Phase 3 ReDiscover‑2 ongoing; selected zovegalisib+atirmociclib triplet for 1L with Phase 3 planned in early 2027.
Cash, cash equivalents and investments were $642.1M at March 31, 2026; Q1 revenue was $3.0M; net loss was $73.3M ($0.41/share).
Relay Therapeutics (Nasdaq: RLAY) will report first quarter 2026 financial results and corporate highlights on Tuesday, May 5, 2026 after U.S. market close. The company is a clinical-stage small molecule precision medicine firm focused on oncology and genetic-disease therapies.
Relay Therapeutics (Nasdaq: RLAY)/b) reported clinical data supporting advancement of into a planned Phase 3 frontline trial for PIK3CA‑mutated, HR+/HER2‑ metastatic breast cancer, targeting initiation in early 2027 pending regulatory feedback.
Key data: 44% ORR (15/34 measurable patients) in median third‑line, 3% zovegalisib discontinuation, 40% grade 3+ TRAE rate, and a pharmacokinetic interaction increasing zovegalisib exposure ~2.5‑fold. Pfizer will supply atirmociclib for the trial.
Relay Therapeutics (Nasdaq: RLAY) will present initial clinical and preclinical data for zovegalisib (RLY-2608) in vascular anomalies at the ISSVA World Congress 2026 in Philadelphia, May 19-22, 2026.
The company expects to report clinical data on approximately 20 efficacy-evaluable patients in a Late Breaking Abstract on May 20, 2026, and will present preclinical murine-model results showing lesion regression with minimal hyperinsulinemia on May 22, 2026. Presentations will be posted on the company website at session start times.
Relay Therapeutics (Nasdaq: RLAY) reported Phase 1/2 ReDiscover data for zovegalisib 400mg BID fed plus fulvestrant in PI3Kα‑mutated, HR+/HER2‑ metastatic breast cancer. Among 57 efficacy‑evaluable patients (data cut‑off Jan 13, 2026) median PFS was 11.1 months (95% CI: 7.3–13.0); ORR was 43% in 35 measurable patients. Pharmacokinetics showed 400mg fed exposures comparable to 600mg fasted. Safety was mainly low‑grade TRAEs; four discontinuations. Zovegalisib has FDA Breakthrough Therapy designation and the Phase 3 ReDiscover‑2 trial is ongoing.
Relay Therapeutics (Nasdaq: RLAY) reported Q4 and full-year 2025 results and outlined 2026 clinical milestones for zovegalisib. Key financials: $554.5M cash and investments at 12/31/25, $15.4M 2025 revenue, and $276.5M net loss for 2025. Clinical highlights include FDA Breakthrough Therapy designation, ESMO TAT presentation on March 16, 2026, and planned 1H 2026 data in PIK3CA-driven vascular anomalies.