A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK) and Preliminary Clinical Activity of RO7673396 in Participants With Advanced Solid Tumors Harboring Rat Sarcoma Viral Oncogene Homolog (RAS) Mutation(s)
Sponsor: Hoffmann-La Roche · NCT06884618 on ClinicalTrials.gov ↗
Conditions studied
What it tests
- RO7673396drug
Where it's running21 sites
- Recruiting now
City of Hope Comprehensive Cancer Center
Duarte, California 91010
- Recruiting now
University of Colorado - Anschutz Medical Campus - PPDS
Aurora, Colorado 80045
- Recruiting now
Smilow Cancer Hospital at Yale New Haven
New Haven, Connecticut 06519-1110
- Recruiting now
Florida Cancer Specialists - Sarasota (North Catttlemen Rd)
Sarasota, Florida 34232
- Recruiting now
MD Anderson Cancer Center
Houston, Texas 77030-3721
- Recruiting now
South Texas Accelerated Research Therapeutics (START)
San Antonio, Texas 78229-4427
15 international sites
- Recruiting now
St Vincent's Hospital Sydney
Darlinghurst, New South Wales, Australia 2010
- Recruiting now
Peter MacCallum Cancer Center
Parkville, Victoria, Australia 3052
- Recruiting now
Princess Margaret Hospital
Toronto, Ontario, Canada M5G 2M9
- Recruiting now
Sun Yat-Sen University Cancer Center - Huangpu Campus
Guangzhou, Guangdong, China 510555
- Recruiting now
Sun Yat-Sen University Cancer Center;Department of Thoracic Surgery
Guangzhou, China 510050
- Recruiting now
Fudan University Shanghai Cancer Center
Shanghai, China 201315
- Recruiting now
Hubei Cancer Hospital
Wuhan, China 430079
- Recruiting now
Rigshospitalet
København Ø, Denmark 2100
- Recruiting now
Prince of Wales Hospital
Hong Kong, Hong Kong
- Recruiting now
New Zealand Clinical Research - Auckland
Auckland, New Zealand 1010
- Recruiting now
New Zealand Clinical Research - Christchurch
Christchurch, New Zealand 8011
- Recruiting now
National Cancer Centre - 30 Hospital Blvd
Singapore, Singapore 168583
- Recruiting now
Clinica Universidad de Navarra
Pamplona, Navarre, Spain 31008
- Recruiting now
National Cheng Kung University Hospital
Tainan, Taiwan 70403
- Recruiting now
National Taiwan University Hospital
Taipei, Taiwan 10002
See the official eligibility language
Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.
Inclusion Criteria: * Histologically documented, locally advanced, recurrent, or metastatic incurable solid tumors * Participants with measurable disease according to RECIST v1.1 assessed by the investigator * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 * Life expectancy ≥12 weeks * Adequate hematologic and end-organ function * Confirmed presence of the RAS mutation(s) Exclusion Criteria: * Current participant or enrollment in another interventional clinical trial * Known hypersensitivity or medical contraindication to any component of RO7673396 formulation * Refractory nausea and vomiting, malabsorption, external biliary shunt, or significant small bowel resection that would preclude adequate study treatment absorption * Known and untreated, or active central nervous system (CNS) metastases * Participants with chronic diarrhea, short bowel syndrome or significant upper gastrointestinal (GI) surgery including gastric resection, a history of inflammatory bowel disease (IBD) * Treatment with chemotherapy, immunotherapy, biologic therapy, or an investigational agent as anti-cancer therapy within 4 weeks or five half-lives prior to initiation of study treatment * Participants who are on acid-reducing agents and unable to safely discontinue them as required in the study * Major surgical procedure within 28 days prior to initiation of study treatment, or incomplete recovery from surgery that would interfere with the determination of safety or efficacy of study treatment, or anticipation of need for a major surgical procedure during the study * Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures * Known clinically significant liver disease
Updated 2026-04-21 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.