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Study Evaluating the Safety and Efficacy of HWK-007, a PTK7-directed Antibody Drug Conjugate in Participants With Advanced Solid Tumors

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NCT07444814 · readout ≤ 804 d

Sponsored by Whitehawk Therapeutics, Inc. (industry) · WHWK — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
226estimated
Sites
12
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-12-19actualWhen the study began enrolling
Primary completionOct 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2028estimatedThe whole study's end, after follow-up
First posted2026-03-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-05actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Endometrial Cancer
  • Ovarian Cancer
  • Ovarian Cancer Metastatic
  • Ovarian Cancer Metastatic Recurrent
  • Non-squamous EGFR Wt NSCLC
  • Platinum Resistant Ovarian Cancer
  • PROC

Intervention

  • Drug: HWK-007 — also filed as HWK-007 anti-PTK7 targeted ADC

Primary outcomes

what the primary-completion date above is the date OF
Determine Maximum Tolerated Dose (MTD)
measured From Cycle 1, Day 1 until Cycle 1, Day 21 (21-day cycles)
Determine Maximum Administered Dose (MAD)
measured From Cycle 1, Day 1 to Cycle 1, Day 21 (21-day cycles) until the MTD is reached.
Determine the Recommended Dose for Expansion (RDE)
measured From Cycle 1, Day 1 to Cycle 1, Day 21 (21-day cycles) until MTD is identified.

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