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NCT01200342 · ClinicalTrials.gov registry record · Phase 2

Genasense, Carboplatin, Paclitaxel (GCP) Combination in Uveal Melanoma

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Terminated
Registry status
Phase 2
Development phase
7
Enrollment target

NCT01200342: Clinical Trial Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT01200342 is a Phase 2 study that was terminated before completion, run by M.D. Anderson Cancer Center. The registered enrollment target is 7 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01200342, a Phase 2 study, was terminated before completion, sponsored by M.D. Anderson Cancer Center.

TERMINATED
Registry status
Phase 2
Development phase
7 participants
Enrollment target

Study Summary

The goal of this clinical research is to learn if the combination of Genasense (oblimersen), carboplatin, and paclitaxel (GCP) can help to control metastatic uveal melanoma. The safety of this combination will also be studied.

Primary Outcome

Tumor response by Response Evaluation Criteria in Solid Tumors for participants with measurable disease defined by presence of at least 1 measurable lesion at baseline: Complete Response (CR): disappearance all target lesions determined by 2 consecutive observations not less than 4 weeks apart. Partial Response (PR): \>30% decrease in sum of LD of target lesions (LD) of target lesions taking as reference baseline sum LD determined by two consecutive observations not less than four weeks apart. P

Interventions

  • DRUG Carboplatin
  • DRUG Paclitaxel
  • DRUG Genasense

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2010-12
Est. Completion 2013-09
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

Why NCT01200342 stopped before completion

NCT01200342 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 3 interventions - of which Carboplatin is the first listed.

NCT01200342 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01200342 about?

NCT01200342 is a clinical study titled "Genasense, Carboplatin, Paclitaxel (GCP) Combination in Uveal Melanoma". The goal of this clinical research is to learn if the combination of Genasense (oblimersen), carboplatin, and paclitaxel (GCP) can help to control metastatic uveal melanoma. The safety of this combination will also be studied.

What is the current status of trial NCT01200342?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 7 participants. The study started on 2010-12. Estimated completion is 2013-09.

What interventions are being tested in trial NCT01200342?

The interventions under investigation include: Carboplatin (DRUG), Paclitaxel (DRUG), Genasense (DRUG).

Who is sponsoring clinical trial NCT01200342?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01200342's enrollment target sits among peer trials

7 1996th of 2000 higher than 5 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01200342, the US trial registry maintained by the National Library of Medicine. NCT01200342 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.