OncRef

Clinical Trial: NCT06848348

Efficacy and Safety Study of Halneuron in the Treatment of Chemotherapy-Induced Neuropathic Pain

Status:

ACTIVE NOT RECRUITING

Phase:

Phase 2

Lead Sponsor:Dogwood Therapeutics Inc.
Information Provided By:Dogwood Therapeutics Inc.
Last Update Posted:2026-09-16

Study Overview

Brief Summary

A randomized study to determine safety and efficacy of a series of subcutaneous (SC) injections of HAL in patients with CINP, compared to matching placebo injections. After that, subjects may have the option to enter an Open Label extension phase, where available, in which all subjects will receive Halneuron.

Official Title

A Randomized, Double-Blind, Placebo Controlled, Multicenter Study With Optional Open-Label Extension to Evaluate the Efficacy and Safety Study of Halneuron in the Treatment of Chemotherapy-Induced Neuropathic Pain

Conditions

Chemotherapy Induced Neuropathic Pain, Chemotherapy Induced Pain Neuropathy, Chemotherapy Induced Pain

Intervention / Treatment

  • Drug: Halneuron
  • Drug: Placebo
  • Drug: Halneuron (Open Label Extension)

Other Study ID Numbers

  • HAL-CINP-203

Start Date (Actual)

2025-02-21

Primary Completion Date (Estimated)

2026-12

Study Completion Date (Estimated)

2026-12

Enrollment (Estimated)

240

Study Type

Interventional

Phase

Phase 2