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Imdelltra (tarlatamab-dlle) demonstrated superior overall survival in small cell lung cancer – Amgen

Written by | 27 Apr 2025

Amgen announced that the global Phase III  DeLLphi-304 clinical trial evaluating Imdelltra (tarlatamab-dlle) as a treatment for patients with small cell lung cancer (SCLC) who progressed on or… read more.

MHRA (UK) has granted a conditional marketing authorisation to Imdylltra (tarlatamab) for the treatment of extensive-stage small cell lung cancer – Amgen

Written by | 14 Feb 2025

Amgen announced that the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has granted a conditional marketing authorisation to Imdylltra for the treatment of adult patients with extensive-stage… read more.

Tepezza (teprotumumab-trbw) receives approval in Japan for the treatment of active thyroid eye disease – Amgen

Written by | 5 Oct 2024

Amgen announced  Tepezza  has been approved for the treatment of active or high clinical activity score (CAS) Thyroid Eye Disease (TED) by Japan’s Ministry of Health, Labour and Welfare (MHLW)…. read more.

FDA approves Bkemv the first interchangeable biosimilar to Soliris (eculizumab) to treat certain rare diseases – Amgen

Written by | 3 Jun 2024

The FDA approved Bkemv (eculizumab-aeeb) as the first interchangeable biosimilar to Soliris (eculizumab) to treat certain rare diseases. Bkemv is approved for the following treatment indications, which are… read more.

FDA approves Imdelltra (taralatamab-dlle),the first and only T cell engager therapy to treatextensive stage small cell lung cancer – Amgen

Written by | 24 May 2024

Amgen announced that the FDA has approved Imdelltra (tarlatamab-dlle) for the treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC) with disease progression on or after… read more.

Amgen to submit MAA to EMA for teprotumumab, to treat moderate to severe thyroid eye disease

Written by | 1 May 2024

Amgeny announced the imminent submission of a Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for teprotumumab, a fully human monoclonal antibody and targeted inhibitor of… read more.

Amgen presents new cardiovascular research at AHA meeting

Written by | 27 Nov 2023

Amgen announced new data reinforcing the safety and efficacy of Repatha (evolocumab) from the FOURIER Open Label Extension (OLE) [FOURIER-OLE] trial at the American Heart Association (AHA) Scientific… read more.

Amgen presents new data that show blood decreases for adults treated with Krystexxa (pegloticase)

Written by | 7 Nov 2023

Amgen announced new data for Krystexxa (pegloticase) showing a decrease in blood pressure during treatment of adults living with chronic gout refractory to oral urate-lowering treatment; uncontrolled gout,… read more.

Additional data from phase IV Tepezza clinical trial presented at the Endocrine Society annual meeting reinforces efficacy in people with thyroid eye disease (TED) regardless of disease activity or duration – Horizon Therapeutics / Amgen

Written by | 23 Jun 2023

Horizon Therapeutics plc announced the presentation of new data from the randomized, double-masked, placebo-controlled Phase IV clinical trial (NCT04583735) evaluating Tepezza in patients with long disease duration and… read more.

Presentation of new Lumakras CODEBREAK 200 CNS data at ASCO 2023 meeting – Amgen

Written by | 9 Jun 2023

Amgen announced the presentation of new data from the CodeBreaK clinical trial program, the most comprehensive global development program in patients with KRAS G12C-mutated cancers, at the American… read more.

New research on Otezla in psoriatic arthritis presented at EULAR 2023 – Amgen

Written by | 29 May 2023

Amgen announced new research examining the use of Otezla (apremilast) in psoriatic arthritis, including the Phase IV MOSAIC study and an exploratory analysis of cardiometabolic risk factors, which… read more.

New data reinforces efficacy of Tezspire in a broad population of severe asthma patients – Amgen

Written by | 22 Apr 2022

Amgen announced results from a pooled post-hoc analysis of the pivotal NAVIGATOR Phase III and PATHWAY Phase IIb trials showed Tezspire (tezepelumab-ekko) demonstrated reductions in the annualized asthma… read more.

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