sexta-feira, 14 de agosto de 2026
PesquisarExplore
Factos em que pode confiar·101 entities·4,772 factos com fonte
Source trace. Via News points to the documents behind its reporting and shows what we drew from each — so you can check any claim. How we source
Source document· January 7, 2026

Merck Initiates Phase 3 KANDLELIT-007 Trial Evaluating Calderasib (MK-1084), an Investigational Oral KRAS G12C Inhibitor, in Combination With KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) in Certain Patients With Advanced NSCLC

View original at finance.yahoo.com
Merck Initiates Phase 3 KANDLELIT-007 Trial Evaluating Calderasib (MK-1084), an Investigational Oral KRAS G12C Inhibitor, in Combination With KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) in Certain Patients With Advanced NSCLC Third Phase 3 trial in Merck’s KANDLELIT clinical development program, whic…
Opening lines of the source · short snapshot — read the full document at the original

O que extraímos desta fonte

The claims Via News extracted from this document. We point to the source; we don't replace it.

  • KRAS is the most frequently mutated oncogene in cancer, and the KRAS G12C mutation occurs in approximately 4% to 14% of all patients with lung cancer globally

    80% confidence
  • Merck operates the largest immuno-oncology clinical research program with over 1,600 trials across multiple cancers

    80% confidence
  • Combination of oral calderasib with subcutaneous KEYTRUDA QLEX will evaluate whether this chemotherapy-free combination requiring no intravenous access may help improve outcomes for patients with KRAS G12C-mutant NSCLC

    80% confidence

Data points we hold from this source

Merck & Co., Inc. · active clinical trials1600 trials
Merck Initiates Phase 3 KANDLELIT-007 Trial Evaluating Calderasib (MK-1084), an Investigational Oral KRAS G12C Inhibitor, in Combination With KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) in Certain Patients With Advanced NSCLC — Source | Via News | pt.VIA.NEWS