Mirati’s First KRAS Data Look At Least As Good As Amgen’s

The small biotech firm has traded higher in recent months based on Amgen’s AMG 510 results to date, and saw its share price soar based on initial efficacy data for MRTX849 in lung and colorectal cancers. 

SC1910_Tree-lungs_246277042_1200.jpg
KRAS G12C mutations are found in 14% of non-small cell lung cancer tumors • Source: Shutterstock

Mirati Therapeutics Inc.’s first-in-human results for the KRAS G12C inhibitor MRTX849 appear to be at least as good as data disclosed to date for Amgen Inc.’s similarly targeted AMG 510 in lung and colorectal cancer patients with KRAS-expressing tumors that have G12C mutations, according to data presented on 28 October at an early stage research meeting hosted by the American Association for Cancer Research, the National Cancer Institute and the European Organisation for Research and Treatment of Cancer. 

Mirati’s results have been closely watched because MRTX849 is only the second drug against KRAS to show efficacy in patients whose tumors harbor this relatively common oncogene, which is...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Clinical Trials

Bayer Has BI In Its Sights With Priority Review For HER2 Lung Cancer Drug

 
• By 

Sevabertinib gets onto the FDA's approval fast track three months after zongertinib.

InflaRx Stock Sinks As Vilobelimab Fails Phase III Skin Trial

 
• By 

A study of the German biotech's intravenous complement factor C5a antibody for pyoderma gangrenosum was stopped for futility.

Angelini Advances Brain Health Ambitions With GRIN Pact

 
• By 

The Italian drugmaker gets rights to Phase III-ready asset radiprodil.

Sweden’s Hansa Slims Down Ahead of Key Readouts

 
• By 

New CEO Renée Aguiar-Lucander is marking her mark.

More from R&D

ASCO Preview: Major Solid Tumor Readouts Include AstraZeneca/Daiichi, Gilead ADCs

 

Data from several closely watched solid tumor drug trials – some considered practice-changing – are scheduled for presentation at the meeting, including for AstraZeneca and Daiichi’s Enhertu.

Gilead Ready To Go After Hepatitis D Again

 
• By 

Following an FDA complete response in 2022, Gilead is getting ready to refile bulevirtide for hepatitis D. The drug already is approved in the EU, UK and elsewhere.

Progress In The Effort To Improve Outcomes In SCLC

 

Several drug makers are working to bring new advances to small-cell lung cancer, a fast-growing cancer with limited treatment options.