Trial · NCT04261387
LUT014 for the Treatment of Radiation Induced Dermatitis in Breast Cancer Patients
NCT04261387, Phase 1, Phase 2, Completed, Lutris Pharma Ltd.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. LUT014 for the Treatment of Radiation Induced Dermatitis in Breast Cancer Patients. Trials, record NCT04261387. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04261387
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- LUT014 for the Treatment of Radiation Induced Dermatitis in Breast Cancer Patients
- NCT number
- NCT04261387
- Status
- Completed
- Phases
- Phase 1, Phase 2
- Enrollment
- 28 participants, actual
- Lead sponsor
- Lutris Pharma Ltd.
- Conditions
- Radiation Dermatitis
- Interventions
- LUT014 Gel, Placebo for LUT014 Gel
- First posted
- 2020-02-07
- Last updated
- 2022-07-27
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of Treatment-Emergent Adverse Events as assessed by CTCAE (Part 1 subjects) | 12 weeks (83 days) | Common Terminology Criteria for Adverse Events Version 5.0 |
| Primary | Change in the severity of radiation dermatitis based on self reporting Dermatology QoL questionnaire (Part 2 subjects) | 14 Days | Dermatology Life Quality Index questionnaire |
| Secondary | Change in the severity of radiation dermatitis assessed by CTCAE (Part 1 subjects) | 12 weeks (83 days) | CTCAE grading scale for dermatitis radiation |
| Secondary | Change in the severity of radiation dermatitis assessed by RTOG/EORTC (part 1 subjects) | 12 weeks (83 days) | Toxicity criteria of the Radiation Therapy Oncology Group (RTOG) and the European Organization for Research and Treatment of Cancer (EORTC) |
| Secondary | Change in the severity of radiation dermatitis based on self reporting Dermatology QoL questionnaire | 12 weeks (83 days) | Dermatology Life Quality Index questionnaire (part 1 subjects) |
| Secondary | Incidence of Treatment-Emergent Adverse Events as assessed by CTCAE (Part 2 subjects) | 12 weeks (83 days) | CTCAE grading scale for dermatitis radiation |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04261387
GET https://conductscience.org/api/trials/v1/NCT04261387/registered