Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02030639 · ClinicalTrials.gov registry record · Phase 1

Metabolism and Excretion of [14C]-Rigosertib After Infusion to Volunteers

A Phase 1 study of Healthy, sponsored by Traws Pharma.

Completed
Registry status
Phase 1
Development phase
6
Enrollment target
1
Study location

NCT02030639: Completed Phase 1 study of Healthy, sponsored by Traws Pharma.

NCT02030639 is a Phase 1 study of Healthy that has completed, run by Traws Pharma. The registered enrollment target is 6 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02030639, a Phase 1 study of Healthy, has completed, sponsored by Traws Pharma.

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to gain an understanding of how the experimental anti-cancer drug, rigosertib, is metabolized in the body and excreted in the urine and feces after it is given as an intravenous infusion. In addition, the study will be carefully monitored to see if any side effects occur. A radioactive drug is used in this study because it is easier and more accurate to measure radioactivity than to use more complicated and less sensitive chemical tests for the drug.

Primary Outcome

Urine sample collection for radio analysis will be over the intervals of 24-30 hours (hr), 30-36 hr, 36-42 hr, 42-48 hr, 48-72 hr, 72-96 hr, 96-120 hr, and if necessary based on discharge criteria, at 120-144 hr, 144-168 hr, 168-192 hr, and 192-216 hr after the infusion start. Fecal sample collection for radio analysis will be over the intervals of 24-30 hr, 30-36 hr, 36-42 hr, 42-48 hr, 48-72 hr, 72-96 hr, 96-120 hr, and if necessary based on discharge criteria, at 120-144 hr, 144-168 hr, 168-1

Conditions Studied

Interventions

  • DRUG rigosertib

Study Locations (1)

Wisconsin

  • Covance Clinical Research Unit, Inc. - Madison

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2014-01
Est. Completion 2015-08
Phase Phase 1
Traws Pharma

25 total trials

What the finished NCT02030639 record still lists

NCT02030639 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 1 intervention - of which rigosertib is the first listed.

NCT02030639 reports a single indexed study location in Wisconsin.

Frequently Asked Questions

What is clinical trial NCT02030639 about?

NCT02030639 is a clinical study titled "Metabolism and Excretion of [14C]-Rigosertib After Infusion to Volunteers". The purpose of this study is to gain an understanding of how the experimental anti-cancer drug, rigosertib, is metabolized in the body and excreted in the urine and feces after it is given as an intravenous infusion. In addition, the study will be carefully monitored to see if any side effects occur...

What is the current status of trial NCT02030639?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2014-01. Estimated completion is 2015-08.

What conditions does trial NCT02030639 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT02030639?

The interventions under investigation include: rigosertib (DRUG).

Who is sponsoring clinical trial NCT02030639?

This trial is sponsored by Traws Pharma, which has 25 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02030639 being conducted?

This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02030639's enrollment target sits among peer trials

6 1075th of 1090 higher than 7 of 1,090 other Healthy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02030639, the US trial registry maintained by the National Library of Medicine. NCT02030639 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.