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Efficacy and Safety of ATX01 in Adult Patients With CIPN (Chemotherapy-induced Peripheral Neuropathy)
NCT05593614 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this clinical trial is to compare the efficacy of twice daily applications of ATX01 (10% \& 15%) versus placebo during a 12-week treatment period in treating chemotherapy-induced peripheral neuropathy (CIPN) in adult cancer survivor patients.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG ATX01 10%
- DRUG ATX01 15%
Study Locations (20)
Other
- OLV Hospital Aalst: gastro-enterologie — Aalst
- Universitair Ziekenhuis Antwerpen — Edegem
- Universitair Ziekenhuis Gent (UZ Gent) — Ghent
- UZ Leuven / Campus Pellenberg / Pain Center — Pellenberg
- CHU UCL Namur - site Godinne — Yvoir
- Clinitrial s.r.o. — Prague
- Praglandia s.r.o. — Prague
- Nemocnice Teplice — Teplice
- Centre Hospitalier de la Côte Basque — Bayonne
- Institute Bergonie — Bordeaux
- CHU de Montpellier, Hôpital Saint Eloi — Montpellier
- Groupe Hospitalier Paris Saint Joseph — Paris
Florida
- South Lake Pain Institute — Clermont
- MGM Medical Care Research & Rehab, LLC — Miami
- Medsol Clinical Research Center, Inc — Port Charlotte
- Knight Neurology - Clinical Research — Rockledge
Kansas
- Neuroscience Research Center, LLC. — Overland Park
Maryland
- The Center for Cancer and Blood Disorders (CCBD) — Bethesda
New York
- University of Rochester Medical Center — Rochester
Texas
- HD Research — Bellaire
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 276 participants |
| Start Date | 2023-02-28 |
| Est. Completion | 2024-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05593614
The ClinicalTrials.gov registry entry for NCT05593614 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 276 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AlgoTherapeutix, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Chemotherapy-induced Peripheral Neuropathy appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05593614 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Other, Florida, Kansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05593614 about?
NCT05593614 is a clinical study titled "Efficacy and Safety of ATX01 in Adult Patients With CIPN (Chemotherapy-induced Peripheral Neuropathy)". The purpose of this clinical trial is to compare the efficacy of twice daily applications of ATX01 (10% \& 15%) versus placebo during a 12-week treatment period in treating chemotherapy-induced peripheral neuropathy (CIPN) in adult cancer survivor patients.
What is the current status of trial NCT05593614?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 276 participants. The study started on 2023-02-28. Estimated completion is 2024-09.
What conditions does trial NCT05593614 study?
This clinical trial studies the following conditions: Chemotherapy-induced Peripheral Neuropathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05593614?
The interventions under investigation include: Placebo (DRUG), ATX01 10% (DRUG), ATX01 15% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05593614?
This trial is sponsored by AlgoTherapeutix, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05593614 being conducted?
This trial has 20 study locations across Florida, Kansas, Maryland, New York, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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