Gilead Set To Expand Trodelvy/Keytruda Into Frontline TNBC

The company reported positive topline results for ASCENT-04, which also bode well for the ASCENT-03 trial in patients with low PD-L1 expression.

• Source: Shutterstock

Gilead Sciences is looking to expand the reach of Trodelvy (sacituzumab govitecan-hziy) into the frontline setting of triple-negative breast cancer (TNBC) based on positive topline results in combination with Merck & Co.’s Keytruda (pembrolizumab). The results are also an encouraging sign for the larger indication of TNBC patients with low PD-L1 expression who are not candidates for checkpoint inhibitors.

Key Takeaways
  • Gilead announced positive topline results from its trial of Trodelvy combined with Keytruda in first-line, PD-L1-positive, inoperable, locally advanced or metastatic triple-negative breast cancer.

Without disclosing numerical data, the Foster City, CA-based drug maker announced 21 April that the Phase III ASCENT-04/KEYNOTE-D19 study showed superior progression-free survival (PFS) for Trodelvy/Keytruda compared with Keytruda combined...

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 Immuno-oncology

Pfizer Scoops 3SBio’s PD-1/VEGF Bispecific In ADC Combo Push

 

Pfizer is doubling down on partnerships for combination therapies involving its antibody-drug conjugates through a new alliance with China's 3SBio’s for a bispecific antibody, potentially worth up to $6bn.

Affimed’s ASCO ‘Hail Mary’ As Survival Chances Slim

 
• By 

The German biotech has been forced into insolvency and NASDAQ suspension.

iTeos/GSK To Terminate Collaboration After TIGIT Trials Flop

 

Belrestotug is the latest anti-TIGIT candidate to fail to meet expectations. iTeos said it will pursue strategic alternatives.

BioNTech Aims To Diversify BNT323 Manufacturing As Filing Nears

 

The company plans to expand manufacturing of the HER2-targeting ADC beyond China and plans to file for US FDA approval in 2025.

More from Scrip

Genentech, Orionis Stick Together In Second Molecular Glue Deal

 

Deal Snapshot: Orionis and Genentech signed a new partnership focused on molecular glues, on top of the one that they struck in 2023.

Finance Watch: Prime, Kyverna, Allogene And More Announce Job Cuts

 
• By 

Restructuring Edition: Prime Medicine ended its sole clinical-stage program to prioritize preclinical and partnered programs, cutting 25% of its workforce to extend its cash runway. Meanwhile, earnings season brought workforce reductions at Kyverna, Allogene, Leap and others.

Merck KGaA Plans Phase III For Enpatoran After Mixed Phase II Lupus Data

 

The Phase II study testing the novel TLR7/8 inhibitor met the primary endpoint in a cohort of patients with cutaneous lupus erythematosus and systemic lupus erythematosus with rash, but did not in patients with SLE.