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Recruiting nowPhase 1Ages 18 Years and up

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

Neoplasms

What it tests

  • RO7673396drug

Where it's running21 sites

  • 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

    Recruiting now
15 international sites
  • 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

    Recruiting now
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.