PipelineReview.com. Biopharmaceutical News & Clinical Trials
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Teva and Alvotech Announce SIMLANDI® (adalimumab-ryvk
May 21, 2024 · SIMLANDI is the first interchangeable high-concentration, citrate-free biosimilar to Humira ®; PARSIPPANY, NJ, USA & REYKJAVÍK, Iceland I May 20, 2024 I Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) and Alvotech (NASDAQ: ALVO),today announced the availability of SIMLANDI (adalimumab-ryvk) injection in the U.S., as an interchangeable ...
Small Molecules - Pipelinereview
Jan 8, 2025 · PipelineReview.com is powered by La Merie Business Intelligence For immediate assistance, please call us during business hours: Mon-Fri 10:00am - 05:00pm; GMT+01 La Merie Publishing - Ulrich Martin Veinat Puigsec - Can Magí s/n | 17862 Vallfogona de Ripollès | Spain | T +34-87-200 1365 | Email [email protected]
Mabwell Announces the CDE Approval of Novel Nectin-4
SHANGHAI, China I August 23, 2024 I Mabwell (688062.SH), an innovative biopharmaceutical company with entire industry chain, announced that its submission to the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) for the “A Randomized, Open-label, Phase III Study to Evaluate 9MW2821 vs Investigator’s Choice of Chemotherapy in Subjects with Recurrent or ...
FDA Approves Genentech’s Tecentriq Hybreza, the First and Only ...
Sep 13, 2024 · – Tecentriq Hybreza provides patients and physicians with greater flexibility of treatment options while showing safety and efficacy consistent with intravenous (IV) Tecentriq –
The race of Keytruda biosimilar antibodies has begun
STUTTGART, Germany I July 28, 2024 I Developed by Merck & Co., the blockbuster therapeutic antibody Keytruda (pembrolizumab) was first approved by the FDA in 2014 to treat several types of cancer. Since getting the initial green light, Keytruda has been approved for new and expanded uses, including melanoma, non-small cell lung cancer, head and …
DATROWAY® Approved in the U.S. for Patients with Previously …
Jan 18, 2025 · TOKYO, Japan & BASKING RIDGE, NJ, USA I January 17, 2055 I DATROWAY ® (datopotamab deruxtecan-dlnk) has been approved in the U.S. for the treatment of adult patients with unresectable or metastatic hormone receptor (HR) positive, HER2 negative (IHC 0, IHC 1+ or IHC 2+/ISH-) breast cancer who have ...
All news - Pipelinereview
4 days ago · BAGSVAERD, Denmark I January 24, 2025 I Novo Nordisk today announced topline results from a phase 1b/2a clinical trial with amycretin, a unimolecular GLP-1 and amylin receptor agonist intended for once weekly subcutaneous administration. The trial investigated the safety, tolerability, pharmacokinetics, and proof-of-concept after once-weekly subcutaneous administrations of amycretin in 125 ...
GSK announces positive phase III results from ANCHOR trials for ...
Oct 14, 2024 · Custom Report. La Merie Publishing offers the service of preparing customized reports tailored to the needs and specifications of the customer. We conduct scientific & medical literature evaluations for clients of the biopharmaceutical industry within the scope of …
Reports - Pipelinereview
Reports Archive - Pipelinereview. PipelineReview.com is powered by La Merie Business Intelligence For immediate assistance, please call us during business hours: Mon-Fri 10:00am - 05:00pm; GMT+01 La Merie Publishing - Ulrich Martin Veinat Puigsec - Can Magí s/n | 17862 Vallfogona de Ripollès | Spain | T +34-87-200 1365 | Email [email protected]