RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

A randomized study to determine safety and efficacy of single subcutaneous (SC) administration of HAL treatment in patients with CINP.

Official Title

A Randomized, Double-Blind, Placebo Controlled, Multicenter, Efficacy and Safety Study of Halneuron in the Treatment of Chemotherapy-Induced Neuropathic Pain

Quick Facts

Study Start:2025-02
Study Completion:2026-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06848348

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Male or female patients aged ≥18 years.
  2. * Neuropathic pain has been present and is attributed to platinum and/or taxane chemotherapy.
  3. * Patient has received a cancer chemotherapy regimen that included taxanes and/or platinum and has no active or discernible disease progression.
  1. * Current neuropathic pain with symptoms similar to CINP but attributed to causes other than platinum or taxane chemotherapy.
  2. * Patients who have received HAL at any time prior to screening.

Contacts and Locations

Study Contact

Dogwood Therapeutics
CONTACT
866-620-9655
Mehran@dwtx.com

Study Locations (Sites)

Ark Clinical Research
Fountain Valley, California, 92708
United States
CenExel ACMR
Atlanta, Georgia, 30331
United States

Collaborators and Investigators

Sponsor: Dogwood Therapeutics Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-02
Study Completion Date2026-08

Study Record Updates

Study Start Date2025-02
Study Completion Date2026-08

Terms related to this study

Keywords Provided by Researchers

  • Neuropathic Pain
  • Chemotherapy
  • Pain

Additional Relevant MeSH Terms

  • Chemotherapy Induced Neuropathic Pain