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NCT02091999 · ClinicalTrials.gov registry record · Phase 1

A Study of Escalating Doses of ASG-22CE Given as Monotherapy in Subjects With Metastatic Urothelial Cancer and Other Malignant Solid Tumors That Express Nectin-4

A Phase 1 study, sponsored by Astellas Pharma Global Development.

Completed
Registry status
Phase 1
Development phase
213
Enrollment target

NCT02091999: Completed Phase 1 study, sponsored by Astellas Pharma Global Development.

NCT02091999 is a Phase 1 study that has completed, run by Astellas Pharma Global Development. The registered enrollment target is 213 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (255% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02091999, a Phase 1 study, has completed, sponsored by Astellas Pharma Global Development.

COMPLETED
Registry status
Phase 1
Development phase
213 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety and pharmacokinetics of enfortumab vedotin as well as assess the immunogenicity and antitumor activity in subjects with metastatic urothelial cancer and other malignant solid tumors that express Nectin-4.

Interventions

  • DRUG enfortumab vedotin

Trial Details

FieldValue
Enrollment Target 213 participants
Start Date 2014-05-14
Est. Completion 2022-12-07
Phase Phase 1
Astellas Pharma Global Development

168 total trials

What the finished NCT02091999 record still lists

NCT02091999 is an interventional study that assigns participants to a tested intervention. The registered 213 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (255% higher).

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

NCT02091999 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02091999 about?

NCT02091999 is a clinical study titled "A Study of Escalating Doses of ASG-22CE Given as Monotherapy in Subjects With Metastatic Urothelial Cancer and Other Malignant Solid Tumors That Express Nectin-4". The purpose of this study is to evaluate the safety and pharmacokinetics of enfortumab vedotin as well as assess the immunogenicity and antitumor activity in subjects with metastatic urothelial cancer and other malignant solid tumors that express Nectin-4.

What is the current status of trial NCT02091999?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 213 participants. The study started on 2014-05-14. Estimated completion is 2022-12-07.

What interventions are being tested in trial NCT02091999?

The interventions under investigation include: enfortumab vedotin (DRUG).

Who is sponsoring clinical trial NCT02091999?

This trial is sponsored by Astellas Pharma Global Development, which has 168 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02091999's enrollment target sits among peer trials

213 245th of 2000 higher than 1,756 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 NCT02091999, the US trial registry maintained by the National Library of Medicine. NCT02091999 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.