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Active Not Recruiting NCT06007937

A Study of Lorlatinib in Combination With Ramucirumab in People With Lung Cancer

Conditions: Non Small Cell Lung Cancer, Metastatic, Recurrent

Sex: All
Ages: 19 Years – N/A
Healthy volunteers: No
Phase: PHASE1, PHASE2
Enrollment: 9
Sponsor: Memorial Sloan Kettering Cancer Center

Location: Memorial Sloan Kettering Monmouth (All Protocol Activities) Middletown New Jersey

Summary

This study will test the safety of the combination of ramucirumab and lorlatinib. The researchers will test one or two different doses of lorlatinib in combination with ramucirumab to find the drug combination dose that causes few or mild side effects in participants. Once the researchers find this dose, they can test it in future participants to see if it is effective in treating their metastatic ALK-rearranged NSCLC. The researchers are also looking to see whether there are specific genes or DNA sequences associated with a response to treatment with lorlatinib and ramucirumab.

Eligibility Criteria

Inclusion Criteria: * Written informed consent * Age \>18 years old * Metastatic or recurrent, biopsy-proven non-small cell lung cancer * ALK fusion identified by next generation sequencing (NGS) or IHC on material obtained from tumor or plasma * Measurable (RECIST 1.1) indicator lesion not previously irradiated * Karnofsky performance status (KPS) ≥ 70% * Adequate organ function defined as follows: ANC ≥1.5 × 10\^9 /L, platelets ≥100 × 10\^9/L, hemoglobin ≥ 9 g/dL, INR ≤ 1.5, PTT or aPTT \

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06007937). StuddyBuddy aggregates publicly available trial information.