Trial · NCT07877155
To Evaluate the Safety and Efficacy of Hemay5394 in Patients With Mild to Moderate Atopic Dermatitis
NCT07877155, Phase 2, Not yet recruiting, Hemay Pharmaceutical PTY. LTD.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. To Evaluate the Safety and Efficacy of Hemay5394 in Patients With Mild to Moderate Atopic Dermatitis. Trials, record NCT07877155. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07877155
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- To Evaluate the Safety and Efficacy of Hemay5394 in Patients With Mild to Moderate Atopic Dermatitis
- NCT number
- NCT07877155
- Status
- Not yet recruiting
- Phases
- Phase 2
- Enrollment
- 90 participants, estimated
- Lead sponsor
- Hemay Pharmaceutical PTY. LTD.
- Conditions
- Safety, Efficiency
- Interventions
- Hemay5394 group, Control group
- First posted
- 2026-10-16
- Last updated
- 2026-10-16
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Proportion of participants achieving Eczema Area and Severity Index (EASI)-75 | Week 4 | |
| Secondary | Proportion of participants with success in the Investigator's Global Assessment for Atopic Dermatitis (vIGA-AD) | Week1,Week2, Week3, Week4, Week6, Week8, and Week9, | |
| Secondary | Proportion of participants with a ≥4-point reduction from baseline in the weekly average of the Worst Itch Numeric Rating Scale (WI-NRS) score | Week1,Week2, Week3, Week4, Week6, Week8, and Week9, | |
| Secondary | Percentage of participants achieving EASI-50 | Week1, Week2, Week3, Week4, Week6, Week8, and Week9 | |
| Secondary | Percentage of participants achieving EASI-75 | Week1, Week2, Week3, Week4,Week6, Week8, and Week9 | |
| Secondary | Percentage of participants achieving EASI-90 | Week1, Week2, Week3, Week4,Week6, Week8, and Week9 | |
| Secondary | Adverse events | through study completion, an average of 9 week | This safety outcome combines the measure of the number of subjects experiencing adverse events (AEs), the nature and severity of those AEs and their relationship to the study treatments. |
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/NCT07877155
GET https://conductscience.org/api/trials/v1/NCT07877155/registered