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EFFICACY AND SAFETY OF DIVARASIB VERSUS SOTORASIB OR ADAGRASIB IN PATIENTS WITH NON-SMALL CELL LUNG CANCER

To evaluate the efficacy of divarasib compared with sotorasib or adagrasib on in patient with non-small cell lung cancer

Age & Gender

  • 18 years ~ 99 years
  • Male, Female

Visit Availability

  • Standard business hours (M-F, 8-5)

Location

United States (Nationwide)

What will be asked of you

At each visit you will get your dose of study pills. You will be asked to take the pills on a daily basis and complete a drug diary. On some visits you will have blood work drawn.

Incentives

Study Drug

In-person visits:
at least 5
Total length of participation:
until disease progression

Looking for Specific Volunteers

Able to participate:

  • Disease progression during or after 1-3 different treatments
  • You have a life expectancy of at least 12 weeks
  • You have an adequate organ function

Not eligible if:

  • You are enrolled on another trial
  • You are pregnant or breastfeeding
  • You are unable to swallow pills

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Primary Visit Location

Lineberger Comprehensive Cancer Center
NC Cancer Hospital (Basnight)
UNC Hospitals / UNC Medical Center
101 Manning Dr, Chapel Hill, NC 27514, USA

Additional Study Information

Principal Investigator

Shetal Patel
LCCC - Clinical Trials

Study Type

Clinical or Medical
Interventional

Study Topics

Cancer (Lung)

IRB Number

24-1290

ClinicalTrials.gov

NCT06497556

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