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Clinical trial

A Phase I , Single Arm, Dose Escalation Study to Evaluate Tolerability, Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 Plus Docetaxel in Patients With KRAS Mutant NSCLC

NCT03990077 is registered in ClinicalTrials.gov with Shanghai Kechow Pharma, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase I , Single Arm, Dose Escalation Study to Evaluate Tolerability, Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 Plus Docetaxel in Patients With KRAS Mutant NSCLC
Lead sponsor
Shanghai Kechow Pharma, Inc.
Phase
Phase 1
Overall status
Terminated
Start date
May 21, 2020
Completion date
July 20, 2021
Enrollment
2 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

nsclc