Predictive Assay for Decision Making in Adjuvant Therapy

TerminatedOBSERVATIONAL
Enrollment

55

Participants

Timeline

Start Date

January 28, 2022

Primary Completion Date

October 28, 2022

Study Completion Date

October 28, 2022

Conditions
Carcinoma, Non-Small-Cell Lung
Interventions
DRUG

Adjuvant

Adjuvant treatment with a standard NSCLC platin-based doublet, 4 cycle (21-day) regimen of the investigator's choice (Arm 1) or other adjuvant therapy (Arm 1a) which can include combination of chemotherapy and targeted therapy, immunotherapy or other.

OTHER

Observation

All patients will be observed for progression free survival and overall survival to the end of study or death, whichever occurs first.

Trial Locations (18)

19104

Penn Presbyterian Medical Center, Philadelphia

20010

MedStar Washington Hospital Center, Washington D.C.

20037

George Washington Medical Faculty Associates, Washington D.C.

22031

Virginia Cancer Specialists, Fairfax

22401

Mary Washington Hospital, Fredericksburg

26506

West Virginia University Medicine, Morgantown

30309

Piedmont Cancer Center, Atlanta

33458

Jupiter Medical Center, Jupiter

53226

Medical College of Wisconsin, Milwaukee

60201

Northshore University Healthsystem, Evanston

66160

The University of Kansas Hospital, Kansas City

70808

Our Lady of the Lake Regional Medical Center, Baton Rouge

76310

Texas Oncology-Wichita Falls Cancer Center, Wichita Falls

78240

Texas Oncology-San Antonio Medical Center, San Antonio

78249

Methodist Healthcare, San Antonio

91010

City of Hope National Medical Center, Duarte

98201

Providence Regional Medical Center Everett, Everett

98683

Peace Health, Vancouver

Sponsors
All Listed Sponsors
collaborator

ClinLogix. LLC

INDUSTRY

lead

Insight Molecular Diagnostics

INDUSTRY

NCT05032352 - Predictive Assay for Decision Making in Adjuvant Therapy | Biotech Hunter | Biotech Hunter