
Solid Tumors Overview
Bayer’s solid tumor research spans multiple molecular targets and signaling pathways, including HER2, KEAP1-NRF2, RAS-PI3Kα, and PRMT5.
Together, these programs represent distinct scientific approaches being investigated across solid tumors, connecting areas of research with compounds in development and their related clinical trials.
6 investigational compounds
7 areas of research
10 clinical trials
Clinical Trials
Tumor Type(s) | Phase | Status | Description | NCT Number |
|---|---|---|---|---|
Lung Cancer, Solid Tumors, Head and Neck Cancer | I | Now Enrolling | A Phase 1, Open-label, Multicenter, First-in-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Anti-tumor Activity of VVD-130037, a Kelch-like ECH Associated Protein 1 (KEAP1) Activator, in Participants With Advanced Solid Tumors | |
Solid Tumors | I | Now Enrolling | A Study to Evaluate the Safety, Pharmacokinetics, and Anti-Tumor Activity of VVD-133214 as Monotherapy and in Combination With Pembrolizumab in Participants With Advanced Solid Tumors | |
Lung Cancer, Solid Tumors, Gastrointestinal Cancer (Colorectal, Pancreatic) | I | Now Enrolling | Phase 1 Study of a SOS1 Inhibitor, BAY 3498264, in Combination in Participants With Advanced KRASG12C-mutated Solid Tumors | |
Lung Cancer, Solid Tumors, Gastrointestinal Cancer (Colorectal, Pancreatic) | I | Now Enrolling | A Phase 1/1b, Open-label, Multicenter, First-in-human Dose Escalation and Dose Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Anti-tumor Activity of VVD-159642, a RAS-PI3Kα Inhibitor, as a Single Agent and in Combination in Participants With Advanced Solid Tumors | |
Solid Tumors | I | Now Enrolling | A Phase 1a, Open-label, Multicenter, Study Evaluating the Safety, Tolerability, Pharmacokinetics and Efficacy of KQB548 in Participants With Advanced Solid Malignancies With a KRAS G12D Mutation | |
Solid Tumors | I, II | Now Enrolling | A First-in-human Study to Evaluate the Safety, Tolerability and Pharmacokinetics, Pharmacodynamics and Preliminary Clinical Activity of BAY 3713372, a Novel 2nd Generation PRMT5 Inhibitor, in Participants With MTAP-deleted Solid Tumors | |
Solid Tumors | I, II | Active, Not Enrolling | A Phase 1/2 Study of the Oral TRK Inhibitor Larotrectinib in Pediatric Patients With Advanced Solid or Primary Central Nervous System Tumors | |
Solid Tumors | II | Now Enrolling | A Phase 2 Open-Label Basket Study to Evaluate the Efficacy and Safety of Orally Administered Reversible Tyrosine Kinase Inhibitor BAY 2927088 in Participants With Metastatic or Unresectable Solid Tumors With HER2-Activating Mutations | |
Solid Tumors | Non-interventional Study | Now Enrolling | Prospective Non-interventional Study in Patients With Locally Advanced or Metastatic TRK Fusion Cancer Treated With Larotrectinib | |
Solid Tumors | Non-interventional Study | Now Enrolling | Special Drug Use Investigation for Larotrectinib |
Bayer’s Oncology Pipeline Brochure
Explore a comprehensive overview of Bayer's oncology pipeline, including investigational compounds, clinical trials, and areas of research.
The ongoing clinical trials listed on this website represent a comprehensive overview of Bayer's clinical pipeline in Oncology, including Bayer-sponsored research and collaborative research with academic centers, cooperative groups, and other global institutions.
HER2, human epidermal growth factor receptor 2; KEAP1, Kelch-like ECH-associated protein 1; KRAS-G12C, Kirsten rat sarcoma viral oncogene homolog with a glycine-to-cysteine substitution at codon 12; KRAS-G12D, Kirsten rat sarcoma viral oncogene homolog with a glycine-to-aspartic acid substitution at codon 12; MAPK, mitogen-activated protein kinase; MTAP, methylthioadenosine phosphorylase; NRF2, nuclear factor erythroid 2–related factor 2; PI3Kα, phosphatidylinositol 3-kinase alpha; PRMT5, protein arginine methyltransferase 5; RAS, rat sarcoma; SOS1, son of sevenless homolog 1; TRK, tropomyosin receptor kinase; WRN, Werner syndrome protein.
