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GSK’s Dostarlimab Gets EU Nod For Endometrial Cancer

 
• By Alexandra Shimmings

While its NDA languishes at the US Food and Drug Administration, the EMA’s CHMP has said yes to dostarlimab’s marketing in the EU for endometrial cancer.    

EU Women Will Soon Have A New Treatment Option For Endometrial Cancer • Source: Shutterstock

GlaxoSmithKline plc is set to get its novel anti-PD-1 product dostarlimab over the line for use in endometrial cancer at last, following a positive opinion from the EMA’s Committee for Medicinal Products for Human Use (CHMP) at its meeting this week.

The product, which will be marketed in the EU as Jemperli (500mg dostarlimab per 10 ml solution for infusion), potentiates...

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In Brief: Nanoscope Ploughs Forward With FDA Application For Retinitis Pigmentosa Gene Therapy

 
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More from Scrip

In Brief: Nanoscope Ploughs Forward With FDA Application For Retinitis Pigmentosa Gene Therapy

 
• By Manas Mishra

Nanoscope’s experimental gene therapy, MCO-010, is designed to target the broader retinitis pigmentosa population, regardless of the underlying gene mutation, with a completed US regulatory submission expected in early 2026.

Stock Watch: Pharma Financial Forecasts Cannot Withstand Headwinds Forever

 
• By Andy Smith

Pharma company financial guidance emerged largely unscathed from a first quarter punctured by a weakening US dollar and threats of import tariffs on drugs. With other pressures either already evident or on the horizon, guidance revisions may be unavoidable.

Q2 Korea Biotech Roundup: Licensing Deals End, Trials Progress, IPOs Recover

 
• By Jung Won Shin

Aside from several sizable global out-licensing deals, South Korean bioventures saw a cancellation of other alliances, updated their pipelines with losses and gains and reported clinical trial progress in the second quarter, while domestic IPO sentiment also improved.