Latest in Pharmaceuticals & Biotech

Pharmaceuticals & Biotech at a glance

The 10 latest articles on Pharmaceuticals & Biotech come from 9 sources, published between Nov 9 and Nov 13. Most come from markets.businessinsider.com (2).

Organizations: FDA (4), U.S. Food and Drug Administration (2), NDA (2), Federal Food (2), NeOnc Technologies Holdings, Inc. (2)

Places: US (2), MD (2)

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Qureight’s fibrosis imaging biomarker selected by Contineum Therapeutics as a secondary endpoint in Phase 2 PROPEL-IPF clinical trial

9 November 2026 Qureight’s Fibr8 model to provide structural assessment as secondary endpoint in Contineum’s Phase 2 PROPEL-IPF clinical trial examining the safety and efficacy of PIPE-791 in idiopathic pulmonary fibrosis (IPF) patients Announcement comes after a recent European Respiratory Journal viewpoint by Qureight…

Genentech’s Divarasib Shows Superiority in Head-to-Head Phase III Trial Against Approved KRAS G12C Inhibitors in Non-Small Cell Lung Cancer

Recent Quotes My Watchlist Indicators Markets Stocks ETFs Tools Markets: Overview News Currencies International Treasuries Genentech’s Divarasib Shows Superiority in Head-to-Head Phase III Trial Against Approved KRAS G12C Inhibitors in Non-Small Cell Lung Cancer By: Genentech via Business Wire July 02, 2026 at…

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NeOnc Technologies Granted FDA Type B End-of-Phase Meeting to Discuss Potential Accelerated Approval Pathway and Phase 3 Confirmatory Trial for Intranasal NEO100

PRESS RELEASE GlobeNewswire Nov. 11, 2026, 08:00 AM CALABASAS, Calif., Nov. 11, 2026 (GLOBE NEWSWIRE) -- NeOnc Technologies Holdings, Inc. (Nasdaq: NTHI) (“NeOnc” or the “Company”), a clinical-stage biopharmaceutical company developing therapies for central nervous system (CNS) cancers, today announced that the U.S. Food and…

Pharmaceuticals & Biotech

Pipelines, trials, approvals, safety, manufacturing, and next‑gen therapies.

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Inside Pharmaceuticals & Biotech

Discovery & Preclinical Targets, assays, animal models, and early safety/tox studies before human trials.
Clinical Trials (Phases I–IV) Design, endpoints, enrollment, interim reads, and post‑market surveillance.
Approvals, Safety & REMS FDA/EMA decisions, boxed warnings, pharmacovigilance, and label changes.
Generics & Biosimilars Access, interchangeability, litigation, and pricing dynamics for follow‑ons.
Vaccines & Immunization Platforms (mRNA, viral vector), boosters, schedules, and cold‑chain supply.
Cell & Gene Therapies CAR‑T, CRISPR, in vivo delivery, manufacturing, and long‑term follow‑up.
Manufacturing & Supply APIs, sterile fill‑finish, shortages, and quality systems across the supply chain.

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