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NCT03340883 · ClinicalTrials.gov registry record · Phase 1

Safety and Tolerability of BION-1301 in Adults With Relapsed or Refractory Multiple Myeloma (MM)

A Phase 1 study, sponsored by Chinook Therapeutics.

Terminated
Registry status
Phase 1
Development phase
21
Enrollment target

NCT03340883: Clinical Trial Phase 1 study, sponsored by Chinook Therapeutics.

NCT03340883 is a Phase 1 study that was terminated before completion, run by Chinook Therapeutics. The registered enrollment target is 21 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03340883, a Phase 1 study, was terminated before completion, sponsored by Chinook Therapeutics.

TERMINATED
Registry status
Phase 1
Development phase
21 participants
Enrollment target

Study Summary

This is a Phase 1/2 study designed to evaluate the safety and tolerability of BION-1301 in adults with relapsed or refractory multiple myeloma whose disease has progressed after 3 or more prior systemic therapies.

Primary Outcome

Number of patients reporting treatment-related adverse events that qualify as dose-limiting toxicities (DLTs) of BION-1301 as a single agent

Interventions

  • BIOLOGICAL BION-1301

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2017-11-15
Est. Completion 2019-07-09
Phase Phase 1
Chinook Therapeutics

4 total trials

Why NCT03340883 stopped before completion

NCT03340883 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower).

The record links to 0 conditions, and to 1 intervention - of which BION-1301 is the first listed.

NCT03340883 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03340883 about?

NCT03340883 is a clinical study titled "Safety and Tolerability of BION-1301 in Adults With Relapsed or Refractory Multiple Myeloma (MM)". This is a Phase 1/2 study designed to evaluate the safety and tolerability of BION-1301 in adults with relapsed or refractory multiple myeloma whose disease has progressed after 3 or more prior systemic therapies.

What is the current status of trial NCT03340883?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2017-11-15. Estimated completion is 2019-07-09.

What interventions are being tested in trial NCT03340883?

The interventions under investigation include: BION-1301 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03340883?

This trial is sponsored by Chinook Therapeutics, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03340883's enrollment target sits among peer trials

21 1615th of 2000 higher than 372 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 NCT03340883, the US trial registry maintained by the National Library of Medicine. NCT03340883 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.