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Phase 1/2 Study of BDTX-1535 in Patients With Glioblastoma or Non-Small Cell Lung Cancer With EGFR

To evaluate the safety, optimum drug usage, and anti tumor activity for the drug BDTX-1535.

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

You will be asked to attend onsite visits to obtain the study drug, if disease progression does not occur, you will return every 21 days to receive treatment. These visits will last until all safety assessments are completed. These assessments includes blood work, vital signs, and medication history.

Incentives

Study Drug

In-person visits:
11+
Phone or online visits:
1
Total length of participation:
Until disease progression

Looking for Specific Volunteers

Able to participate:

  • Have disease progression with prior treatments
  • Have advanced/metastatic non-small cell lung cancer
  • Life expectancy of at least 3 months

Not eligible if:

  • Significant cardiovascular disease
  • Received other recent antitumor therapy
  • Major surgery within 4 weeks before first dose of study drug or scheduled for surgery during projected course of the study.

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

24-0821

ClinicalTrials.gov

NCT05256290

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