Clinical trial
A Phase I, Single Arm, Dose Escalation Study to Evaluate Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 in Subjects With Advanced Solid Tumors
NCT03976050 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 Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 in Subjects With Advanced Solid Tumors
- Lead sponsor
- Shanghai Kechow Pharma, Inc.
- Phase
- Phase 1
- Overall status
- Terminated
- Start date
- June 17, 2019
- Completion date
- November 12, 2020
- Enrollment
- 4 (actual)
- Sites
- 2
Conditions
As the registry lists them; a condition with its own page is linked.
solid tumor, adult