Screening Study for Participants With Malignant Tumors
- Conditions
- Solid Tumors
- Registration Number
- NCT05419375
- Lead Sponsor
- Hoffmann-La Roche
- Brief Summary
The study objective is to determine the biomarker status of a participant's tumor tissue and use that status to determine eligibility for a linked Roche clinical trial.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 15000
- Confirmed availability of a representative formalin-fixed, paraffin-embedded (FFPE) tumor specimen meeting criteria defined in the protocol
- Considered by principal investigator (PI) to be a candidate for a linked clinical trial with an investigational medicinal product, and that the participant has the awareness and willingness to participate in said trial
Inclusion Criteria for Participants with Stage III NSCLC
- Locally advanced, unresectable Stage III NSCLC of either squamous or non-squamous histology based on 8th edition of the American Joint Committee on Cancer (AJCC) and Union for International Cancer Control (UICC) cancer staging system
- Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
Inclusion Criteria for Participants with Stage II, IIIA, or Select IIIB (T3N2 only) NSCLC Requiring Adjuvant Treatment
- Stage II, IIIA, or select IIIB (T3N2 only) NSCLC based on the 8th edition of the AJCC and UICC cancer staging system (Amin et al. 2017)
- Considered eligible for curative intent surgery (complete resection with all surgical margins testing negative for tumor)
- Screening within Study BX43361, using a pretreatment biopsy, is encouraged to be performed as early in the participant treatment pathway as possible to ensure the participant is potentially eligible for all cohorts, and should meet guidelines as defined by the protocol
- Representative FFPE tumor specimen obtained prior to the start of any treatment
- ECOG Performance Status of 0 or 1
General
- History of malignancy other than NSCLC within 5 years prior to screening, except for malignancies with a negligible risk of metastasis or death
- Any condition that may affect the interpretation of study results
- Significant liver or cardiovascular disease
- Prior allogenic stem-cell or solid-organ transplantation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Proportion of participants eligible for a linked Roche clinical trial Up to 10 years Proportion of participants with evaluable biomarker results Up to 10 years
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (159)
Arizona Oncology Associates, PC - HOPE
🇺🇸Tucson, Arizona, United States
Southern California Kaiser Permanente
🇺🇸San Diego, California, United States
Rocky Mountain Cancer Centers-Penrose Pavillion
🇺🇸Longmont, Colorado, United States
Oregon Health Sciences Uni
🇺🇸Portland, Oregon, United States
Hillman Cancer Center
🇺🇸Pittsburgh, Pennsylvania, United States
Thompson Cancer Survival Center
🇺🇸Knoxville, Tennessee, United States
Baptist Cancer Center
🇺🇸Memphis, Tennessee, United States
Texas Oncology, P.A.
🇺🇸San Antonio, Texas, United States
Mays Cancer Center, UT Health San Antonio
🇺🇸San Antonio, Texas, United States
Texas Oncology- Northeast Texas
🇺🇸Tyler, Texas, United States
Scroll for more (149 remaining)Arizona Oncology Associates, PC - HOPE🇺🇸Tucson, Arizona, United States