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Avidity Biosciences Enters into Agreement to be Acquired by Novartis AG

Avidity Biosciences Enters into Agreement to be Acquired by Novartis AG

✨ Onyx Summary Avidity Biosciences (Nasdaq: RNA) entered into a definitive agreement to be acquired by Novartis AG for $72.00 per share in cash, valuing Avidity at approximately $12 billion, following the planned spin-off of its early-stage precision cardiology programs into a new public company, SpinCo. The transaction, unanimously approved

Guardant Health to Share Data Supporting Critical Role of Blood-Based Testing in Improving Cancer Screening Adherence at ACG 2025

Guardant Health to Share Data Supporting Critical Role of Blood-Based Testing in Improving Cancer Screening Adherence at ACG 2025

✨ Onyx Summary Guardant Health (Nasdaq: GH) announced new data to be presented at the 2025 American College of Gastroenterology Annual Meeting demonstrating that its FDA-approved Shield blood test achieved over 90% adherence for colorectal cancer screening, significantly higher than traditional methods. The company also shared survey findings showing patient preference

Kyverna Therapeutics Highlights Potential of KYV-101 in Rheumatoid Arthritis with Phase 1 Data from Investigator-Initiated Trial Presented at ACR Convergence 2025

Kyverna Therapeutics Highlights Potential of KYV-101 in Rheumatoid Arthritis with Phase 1 Data from Investigator-Initiated Trial Presented at ACR Convergence 2025

✨ Onyx Summary Kyverna Therapeutics (Nasdaq: KYTX) reported positive Phase 1 results from an investigator-initiated trial of KYV-101, its CD19 CAR T-cell therapy, in treatment-refractory rheumatoid arthritis, showing strong CAR T-cell expansion, full B-cell depletion, and meaningful clinical responses with no high-grade adverse events. Presented by Charité – University of Berlin at

Phathom Pharmaceuticals Announces Publication of Data from Phase 3 pHalcon-NERD-301 Study Showing VOQUEZNA® (vonoprazan) Improved Nocturnal GERD Symptoms in Patients with Non-Erosive Reflux Disease

Phathom Pharmaceuticals Announces Publication of Data from Phase 3 pHalcon-NERD-301 Study Showing VOQUEZNA® (vonoprazan) Improved Nocturnal GERD Symptoms in Patients with Non-Erosive Reflux Disease

✨ Onyx Summary Phathom Pharmaceuticals (Nasdaq: PHAT) announced the publication of additional analyses from its Phase 3 pHalcon-NERD-301 trial in The American Journal of Gastroenterology, demonstrating that VOQUEZNA® (vonoprazan) significantly improved nighttime reflux symptoms in patients with Non-Erosive Reflux Disease (NERD). The results highlight VOQUEZNA’s sustained nocturnal symptom relief and

Lilly to Acquire Adverum Biotechnologies

Lilly to Acquire Adverum Biotechnologies

✨ Onyx Summary Eli Lilly and Company (NYSE: LLY) announced a definitive agreement to acquire Adverum Biotechnologies (Nasdaq: ADVM) and its lead gene therapy candidate, Ixo-vec, for up to $12.47 per share, including $3.56 in cash and a contingent value right worth up to $8.91 based on future

Phathom Pharmaceuticals to Highlight VOQUEZNA® (vonoprazan) at the American College of Gastroenterology (ACG) 2025 Annual Scientific Meeting

Phathom Pharmaceuticals to Highlight VOQUEZNA® (vonoprazan) at the American College of Gastroenterology (ACG) 2025 Annual Scientific Meeting

✨ Onyx Summary Phathom Pharmaceuticals (Nasdaq: PHAT) announced its participation at the 2025 American College of Gastroenterology Annual Scientific Meeting, where it will highlight VOQUEZNA® (vonoprazan) as an approved treatment for gastroesophageal reflux disease (GERD) through a product theater presentation and exhibit booth engagement. The company aims to strengthen its leadership

Nuvation Bio Enrolls First Patient in Global, Randomized Study of Safusidenib for Maintenance Treatment of High-Grade IDH1-Mutant Glioma

Nuvation Bio Enrolls First Patient in Global, Randomized Study of Safusidenib for Maintenance Treatment of High-Grade IDH1-Mutant Glioma

✨ Onyx Summary Nuvation Bio (NYSE: NUVB) announced the enrollment of the first patient in Part 2 of its global G203 trial evaluating safusidenib, an oral IDH1 inhibitor, as maintenance therapy for high-grade IDH1-mutant astrocytoma following standard treatment. The study, now expanding into a Phase 3 registration trial with approximately 300

Geron Corporation Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Geron Corporation Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

✨ Onyx Summary Geron Corporation (Nasdaq: GERN) granted inducement equity awards totaling approximately 3.08 million shares to four newly hired employees, including stock options and restricted stock units, under its 2018 Inducement Award Plan. The awards, approved by the Board’s Compensation Committee pursuant to Nasdaq Rule 5635(c)(4)

Perspective Therapeutics Presents Updated Interim Data from its Ongoing Phase 1/2a Clinical Trial of [212Pb]VMT-α-NET at the ESMO Congress 2025

Perspective Therapeutics Presents Updated Interim Data from its Ongoing Phase 1/2a Clinical Trial of [212Pb]VMT-α-NET at the ESMO Congress 2025

✨ Onyx Summary Perspective Therapeutics (NYSE American: CATX) reported updated interim results from its ongoing Phase 1/2a trial of [212Pb]VMT-α-NET in patients with unresectable or metastatic SSTR2-expressing neuroendocrine tumors, showing strong tolerability with no dose-limiting toxicities and encouraging anti-tumor activity, including confirmed responses in 44% of patients with uniform

Verily Launches a New Consumer Health App, Verily Me, at HLTH USA 2025

Verily Launches a New Consumer Health App, Verily Me, at HLTH USA 2025

✨ Onyx Summary Verily announced the launch of Verily Me, a new consumer health app showcased at HLTH USA 2025, designed to integrate clinical insights, personal health data, and AI assistance to help users manage their health and close care gaps. Built on Verily’s precision health platform and linked to