Latest in Pharmaceuticals & Biotech

prnewswire.com
1,014 words

AbbVie Presents Long-Term RINVOQ® (upadacitinib) Data Showing Continued Repigmentation in Non-Segmental Vitiligo

Oct 01, 2026, 10:00 ET NORTH CHICAGO, Ill., Oct. 1, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced late-breaking results from the ongoing Phase 3 Viti-Up-1 and Viti-Up-2 studies of RINVOQ® (upadacitinib; 15 mg once daily) in non-segmental vitiligo (NSV), showing continued facial and total body repigmentation through week…

kidney.org
1,722 words

Diet After Kidney Transplant

Tune in for the latest research and perspectives on kidney health from NKF. Answer a few questions and we will provide you with information about your kidney health. Learn about the basics of kidney disease, how it is measured, and…

marketscreener.com
229 words

Lakewood-Amedex Biotherapeutics Inc. Announces Positive Minimum Inhibitory Concentration Data From Recent Clinical Isolates For Nu-3

Lakewood-Amedex Biotherapeutics Inc. announced positive Minimum Inhibitory Concentration data from recent clinical isolates for its lead clinical candidate, Nu-3. Nu-3 is currently being investigated... announced positive Minimum Inhibitory Concentration (MIC) data from recent clinical isolates for its lead clinical candidate, Nu…

marketscreener.com
46 words

Lakewood-Amedex Biotherapeutics announces positive data for the advancement of lead candidate, Nu-3

Lakewood-Amedex Biotherapeutics Inc: Lakewood-Amedex Biotherapeutics announces positive data for the advancement of lead candidate, Nu-3, in infected diabetic foot ulcers Lakewood-Amedex... Biotechnology & Medical Research Lakewood-Amedex Biotherapeutics announces positive data for the advancement of lead candidate, Nu-3 Published on 05/18/2026 at 09:38 am…

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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