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NCT01522664 · ClinicalTrials.gov registry record · Phase 1

A Study of DEDN6526A in Patients With Metastatic or Unresectable Melanoma

A Phase 1 study, sponsored by Genentech.

Completed
Registry status
Phase 1
Development phase
53
Enrollment target

NCT01522664: Completed Phase 1 study, sponsored by Genentech.

NCT01522664 is a Phase 1 study that has completed, run by Genentech. The registered enrollment target is 53 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (12% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01522664, a Phase 1 study, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 1
Development phase
53 participants
Enrollment target

Study Summary

This multicenter, open-label study will assess the safety and pharmacokinetics of DEDN6526A in patients with metastatic or unresectable melanoma. Cohorts of patients will receive escalating doses of DEDN6526A by intravenous infusion on Day 1 of each 21-day cycle. In the absence of disease progression or unacceptable toxicity, patients may continue to receive DEDN6552A for up to 17 cycles (1 year).

Interventions

  • DRUG DEDN6526A

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2012-03
Est. Completion 2015-06
Phase Phase 1
Genentech

332 total trials

What the finished NCT01522664 record still lists

NCT01522664 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 53 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (12% lower).

The record links to 0 conditions, and to 1 intervention - of which DEDN6526A is the first listed.

NCT01522664 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01522664 about?

NCT01522664 is a clinical study titled "A Study of DEDN6526A in Patients With Metastatic or Unresectable Melanoma". This multicenter, open-label study will assess the safety and pharmacokinetics of DEDN6526A in patients with metastatic or unresectable melanoma. Cohorts of patients will receive escalating doses of DEDN6526A by intravenous infusion on Day 1 of each 21-day cycle. In the absence of disease progressio...

What is the current status of trial NCT01522664?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 53 participants. The study started on 2012-03. Estimated completion is 2015-06.

What interventions are being tested in trial NCT01522664?

The interventions under investigation include: DEDN6526A (DRUG).

Who is sponsoring clinical trial NCT01522664?

This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01522664's enrollment target sits among peer trials

53 948th of 2000 higher than 1,045 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01522664, the US trial registry maintained by the National Library of Medicine. NCT01522664 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.