Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03872206 · ClinicalTrials.gov registry record · Phase 1

Study of HPN536 in Patients With Advanced Cancers Associated With Mesothelin Expression

A Phase 1 study, sponsored by Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA).

Completed
Registry status
Phase 1
Development phase
95
Enrollment target

NCT03872206 is a Phase 1 study that has completed, run by Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA). The registered enrollment target is 95 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03872206, a Phase 1 study, has completed, sponsored by Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA).

COMPLETED
Registry status
Phase 1
Development phase
95 participants
Enrollment target

Study Summary

An open-label, Phase 1/2a study of HPN536 as monotherapy to assess the safety, tolerability and PK in patients with advanced cancers associated with mesothelin expression.(Phase 2 portion of the study was not conducted.)

Interventions

  • BIOLOGICAL HPN536 Fixed IV 6 to 560 ng/kg
  • BIOLOGICAL HPN536 1 Prime Step IV 600-1200 ng/kg Target
  • BIOLOGICAL 2 Prime Step IV 900-14000 ng/kg Target

Trial Details

FieldValue
Enrollment Target 95 participants
Start Date 2019-04-16
Est. Completion 2023-01-04
Phase Phase 1

What the Registry Record Tells You About NCT03872206

The ClinicalTrials.gov registry entry for NCT03872206 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 95 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 4 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which HPN536 Fixed IV 6 to 560 ng/kg is the first listed.

NCT03872206 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03872206 about?

NCT03872206 is a clinical study titled "Study of HPN536 in Patients With Advanced Cancers Associated With Mesothelin Expression". An open-label, Phase 1/2a study of HPN536 as monotherapy to assess the safety, tolerability and PK in patients with advanced cancers associated with mesothelin expression.(Phase 2 portion of the study was not conducted.)

What is the current status of trial NCT03872206?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 95 participants. The study started on 2019-04-16. Estimated completion is 2023-01-04.

What interventions are being tested in trial NCT03872206?

The interventions under investigation include: HPN536 Fixed IV 6 to 560 ng/kg (BIOLOGICAL), HPN536 1 Prime Step IV 600-1200 ng/kg Target (BIOLOGICAL), 2 Prime Step IV 900-14000 ng/kg Target (BIOLOGICAL).

Who is sponsoring clinical trial NCT03872206?

This trial is sponsored by Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA), which has 4 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.