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NCT03642990 · ClinicalTrials.gov registry record · Phase 2

NR in Chemo-induced Peripheral Neuropathy

A Phase 2 study, sponsored by Donna Hammond, PhD.

Terminated
Registry status
Phase 2
Development phase
5
Enrollment target

NCT03642990: Clinical Trial Phase 2 study, sponsored by Donna Hammond, PhD.

NCT03642990 is a Phase 2 study that was terminated before completion, run by Donna Hammond, PhD. The registered enrollment target is 5 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03642990, a Phase 2 study, was terminated before completion, sponsored by Donna Hammond, PhD.

TERMINATED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

The purpose of this single-arm phase II trial is to determine whether nicotinamide riboside (NIAGEN®) prevents the progression of peripheral sensory neuropathy in patients receiving infusions of paclitaxel or nab-paclitaxel for the treatment of metastatic breast cancer or recurrent platinum-resistant ovarian, endometrial, peritoneal, fallopian tube cancer or metastatic head and neck cancer.

Primary Outcome

The primary outcome variable is defined as no worsening of the grade of peripheral sensory neuropathy as scored according to the Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 guidelines. Per the CTCAE a score of 1 would be assigned in the instance of parethesias or a loss of deep tendon reflexes. A score of 2 would be assigned in the instance of moderate symptoms that limit instrumental activities of daily living. A score of 3 would be assigned in the instance of severe sym

Interventions

  • DRUG Nicotinamide Riboside

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2019-11-08
Est. Completion 2022-02-24
Phase Phase 2
Donna Hammond, PhD

2 total trials

Why NCT03642990 stopped before completion

NCT03642990 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower).

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

NCT03642990 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03642990 about?

NCT03642990 is a clinical study titled "NR in Chemo-induced Peripheral Neuropathy". The purpose of this single-arm phase II trial is to determine whether nicotinamide riboside (NIAGEN®) prevents the progression of peripheral sensory neuropathy in patients receiving infusions of paclitaxel or nab-paclitaxel for the treatment of metastatic breast cancer or recurrent platinum-resistan...

What is the current status of trial NCT03642990?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2019-11-08. Estimated completion is 2022-02-24.

What interventions are being tested in trial NCT03642990?

The interventions under investigation include: Nicotinamide Riboside (DRUG).

Who is sponsoring clinical trial NCT03642990?

This trial is sponsored by Donna Hammond, PhD, which has 2 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03642990's enrollment target sits among peer trials

5 2000th of 2000 the lowest 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 NCT03642990, the US trial registry maintained by the National Library of Medicine. NCT03642990 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.