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A Study of Mipasetamab Uzoptirine (ADCT-601) in Participants With Solid Tumors

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NCT05389462

Sponsored by ADC Therapeutics S.A. (industry) · ADCT — their whole pipeline →.

Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
128actual
Sites
14
Countries
France, Spain, United Kingdom +1

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

Why the sponsor stopped it

Sponsor decided to halt further development of ADCT-601

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-07-13actualWhen the study began enrolling
Primary completion2025-04-17actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-04-17actualThe whole study's end, after follow-up
First posted2022-05-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-05-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced Solid Tumors

Interventions

  • Drug: ADCT-601 — also filed as Mipasetamab uzoptirine
  • Drug: Gemcitabine

Primary outcomes

what the primary-completion date above is the date OF
Safety and Tolerability as Assessed by Number of Participants with Adverse Events (AEs)
measured Up to approximately 2 years
Number of Participants who Experience a Dose Limiting Toxicity (DLT)
measured Day 1 to Day 21
Number of Participants who Experience a Dose Interruption
measured Up to approximately 2 years
Number of Participants who Experience a Dose Reduction
measured Up to approximately 2 years

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