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NCT02649790 · ClinicalTrials.gov registry record · Phase 1

Study of the Safety, Tolerability and Efficacy of KPT-8602 in Participants With Relapsed/Refractory Cancer Indications

A Phase 1 study, sponsored by Karyopharm Therapeutics.

Completed
Registry status
Phase 1
Development phase
277
Enrollment target

NCT02649790: Completed Phase 1 study, sponsored by Karyopharm Therapeutics.

NCT02649790 is a Phase 1 study that has completed, run by Karyopharm Therapeutics. The registered enrollment target is 277 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (362% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02649790, a Phase 1 study, has completed, sponsored by Karyopharm Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
277 participants
Enrollment target

Study Summary

This is a first-in-human, multi-center, open-label clinical study with separate dose escalation (Phase 1) and expansion (Phase 2) stages to assess preliminary safety, tolerability, and efficacy of the second generation oral XPO1 inhibitor KPT-8602 in participants with relapsed/refractory multiple myeloma (MM), metastatic colorectal cancer (mCRC), metastatic castration resistant prostate cancer (mCRPC), higher risk myelodysplastic syndrome (HRMDS), acute myeloid leukemia (AML) and newly diagnosed intermediate/high-risk MDS. Dose escalation and dose expansion may be included for all parts of the study as determined by ongoing study results.

Interventions

  • DRUG Dexamethasone
  • DRUG ASTX727
  • DRUG KPT-8602

Trial Details

FieldValue
Enrollment Target 277 participants
Start Date 2016-01
Est. Completion 2024-12-23
Phase Phase 1
Karyopharm Therapeutics

25 total trials

What the finished NCT02649790 record still lists

NCT02649790 is an interventional study that assigns participants to a tested intervention. The registered 277 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 (362% higher).

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

NCT02649790 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02649790 about?

NCT02649790 is a clinical study titled "Study of the Safety, Tolerability and Efficacy of KPT-8602 in Participants With Relapsed/Refractory Cancer Indications". This is a first-in-human, multi-center, open-label clinical study with separate dose escalation (Phase 1) and expansion (Phase 2) stages to assess preliminary safety, tolerability, and efficacy of the second generation oral XPO1 inhibitor KPT-8602 in participants with relapsed/refractory multiple my...

What is the current status of trial NCT02649790?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 277 participants. The study started on 2016-01. Estimated completion is 2024-12-23.

What interventions are being tested in trial NCT02649790?

The interventions under investigation include: Dexamethasone (DRUG), ASTX727 (DRUG), KPT-8602 (DRUG).

Who is sponsoring clinical trial NCT02649790?

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

How this trial's enrollment target compares

Where NCT02649790's enrollment target sits among peer trials

277 147th of 2000 higher than 1,853 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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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT02649790, the US trial registry maintained by the National Library of Medicine. NCT02649790 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.