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NCT05807113
Assessment of Skin Tolerance and Efficacy of a Cosmetic Product After 5 Days of Use on Subjects With Atopic Dermatitis
NA trial testing Atopi intensive care BNO 3731 in Atopic Diathesis in 44 participants. Completed in 22 February 2022.
22 February 2022
Quick facts
| Lead sponsor | Bionorica SE |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | other |
| Enrollment | 44 |
| Start date | 15 February 2022 |
| Primary completion | 22 February 2022 |
| Estimated completion | 22 February 2022 |
| Sites | 1 location across Germany |
Drugs / interventions tested
- Atopi intensive care BNO 3731
- Benchmark product
Conditions studied
- Atopic Diathesis — all drugs for Atopic Diathesis →
- Eczema-prone Skin — all drugs for Eczema-prone Skin →
Sponsor
Bionorica SE — full company profile →
Who can join
Adults 6 Months to 65, any sex, with Atopic Diathesis or Eczema-prone Skin. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of this study is to compare the efficacy and tolerability and of a cosmetic product to one that is already available on the market (benchmark product). Efficacy is assessed by instrumental measurements of skin condition, clinical examinations, and questionnaires.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Clinical Measurement of Transepidermal Water Loss.
Kundu D, Jayaraman A, Sen CK. · · 2026 · cited 4× · PMID 40476522 · DOI 10.1089/wound.2024.0148
Verify or expand the search:
- PubMed search for NCT05807113
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Bionorica SE trials
Trials by the same sponsor.
- NCT06211049 — Efficacy of Vitex Agnus-castus BNO 1095 (20 mg) in Women With Primary Dysmenorrhea · Phase 3 · completed
- NCT05790083 — Skin Efficacy and Tolerability of a Cosmetic Product Combination Over 3 Months in Subjects With Atopic Eczema · NA · unknown
- NCT05786976 — Assessment of Skin Tolerance and Efficacy of a Cosmetic Product After 4 Weeks of Use on Subjects With Atopic Dermatitis · NA · completed
- NCT03756974 — BX-1 in Spasticity Due to Multiple Sclerosis · Phase 3 · completed
- NCT02746042 — Sinupret Extract Coated Tablets in Chronic Rhinosinusitis · Phase 3 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05807113 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Bionorica SE
- Last refreshed: 11 April 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05807113.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing