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NCT06848348Active, not recruitingPhase 2

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

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

Source: ClinicalTrials.gov · Last updated 16 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
240 (estimated)
First submitted
3 Feb 2025
Start date
21 Feb 2025
Primary completion date
Dec 2026
Lead sponsor
Dogwood Therapeutics Inc.
NCT number
NCT06848348

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 240
  • From 21 Feb 2025 to the primary completion date, Dec 2026
  • 24 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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.

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (24)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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Fair OaksUnited StatesUnknown status
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FentonUnited StatesUnknown status
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Fountain ValleyUnited StatesUnknown status
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Garden CityUnited StatesUnknown status
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GlendaleUnited StatesUnknown status
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GurneeUnited StatesUnknown status
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HoustonUnited StatesUnknown status
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JacksonvilleUnited StatesUnknown status
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Lake CharlesUnited StatesUnknown status
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LakelandUnited StatesUnknown status
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Las VegasUnited StatesUnknown status
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Los AngelesUnited StatesUnknown status
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MadisonUnited StatesUnknown status
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McAllenUnited StatesUnknown status
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OrlandoUnited StatesUnknown status
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PhoenixUnited StatesUnknown status
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Port CharlotteUnited StatesUnknown status
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Salt Lake CityUnited StatesUnknown status
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Santa RosaUnited StatesUnknown status
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SheffieldUnited StatesUnknown status
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TampaUnited StatesUnknown status
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Wheat RidgeUnited StatesUnknown status
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WilliamsvilleUnited StatesUnknown status
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Winston-SalemUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.