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

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

Recruiting
18 years and older
All
Phase 2
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Overview

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

Eligibility

Inclusion Criteria:

  • Male or female patients aged ≥18 years.
  • Neuropathic pain has been present and is attributed to platinum and/or taxane chemotherapy.
  • Patient has received a cancer chemotherapy regimen that included taxanes and/or platinum and has no active or discernible disease progression.

Exclusion Criteria:

  • Current neuropathic pain with symptoms similar to CINP but attributed to causes other than platinum or taxane chemotherapy.
  • Patients who have received HAL at any time prior to screening.

Study details
    Chemotherapy Induced Neuropathic Pain

NCT06848348

Dogwood Therapeutics Inc.

20 April 2025

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