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NCT03030885 · ClinicalTrials.gov registry record · Phase 1

Use of an Experimental Radiopharmaceutical (131I-MIP-1095) in Men With Metastatic Castration-Resistant Prostate Cancer (mCRPC)

A Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
10
Enrollment target

NCT03030885: Completed Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT03030885 is a Phase 1 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 10 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03030885, a Phase 1 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
10 participants
Enrollment target

Study Summary

The main purpose of this study to determine the safety of an experimental medicine called 131I-MIP-1095. 131I-MIP-1095 is an investigational drug, meaning it has not been approved by the U.S. Food \& Drug Administration (FDA).

Primary Outcome

This is a phase 1 dose escalation study of 131I-MIP-1095 in men with metastatic castration-resistant prostate cancer. There are a maximum of five doses under consideration. Dose escalation cohorts will be studied if acceptable toxicity is observed. A dose limiting toxicity is defined as the occurrence of any of the following drug-related toxicities during the first cycle.

Interventions

  • DRUG 131I-MIP-1095

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2017-01-19
Est. Completion 2019-04-02
Phase Phase 1
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT03030885 record still lists

NCT03030885 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 1 intervention - of which 131I-MIP-1095 is the first listed.

NCT03030885 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03030885 about?

NCT03030885 is a clinical study titled "Use of an Experimental Radiopharmaceutical (131I-MIP-1095) in Men With Metastatic Castration-Resistant Prostate Cancer (mCRPC)". The main purpose of this study to determine the safety of an experimental medicine called 131I-MIP-1095. 131I-MIP-1095 is an investigational drug, meaning it has not been approved by the U.S. Food \& Drug Administration (FDA).

What is the current status of trial NCT03030885?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2017-01-19. Estimated completion is 2019-04-02.

What interventions are being tested in trial NCT03030885?

The interventions under investigation include: 131I-MIP-1095 (DRUG).

Who is sponsoring clinical trial NCT03030885?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03030885's enrollment target sits among peer trials

10 1913th of 2000 higher than 46 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 NCT03030885, the US trial registry maintained by the National Library of Medicine. NCT03030885 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.