Mode
Text Size
Log in / Sign up
Phase 2 N=24 Randomized Single-blind Treatment

Safety and Efficacy of CD10367 in Psoriasis Vulgaris

Psoriasis Vulgaris

Enrolled (actual)
24
Serious AEs
0.0%
Results posted
Sep 2024
Primary outcome: Primary: Area Under the Curve (AUC) of Total Sum Score (Sum of Erythema, Scaling and Induration Scores) — 103.4; 101.7; 118.0; 118.6 score on a scale*days

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
CD10367 3% Solution - Non-desquamated zone (Drug); CD10367 1% Solution - Non-desquamated zone (Drug); CD10367 solution placebo - Non-desquamated zone (Drug); Betneval ointment - Non-desquamated zone (Drug); CD10367 3% Solution - Desquamated zone (Drug); CD10367 solution placebo - Desquamated zone (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Galderma R&D
Primary completion
Mar 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Area Under the Curve (AUC) of Total Sum Score (Sum of Erythema, Scaling and Induration Scores)
103.4; 101.7; 118.0; 118.6; 116.6; 75.3
SECONDARY
Area Under the Curve (AUC) of Individual Clinical Scores
37.1; 37.7; 42.7; 41.3; 41.7; 27.2
SECONDARY
Total Sum Score (TSS) of Individual Clinical Scores
5.0; 5.0; 7.3; 7.3; 7.3; 7.2
SECONDARY
Percent Change in Total Sum Score (TSS)
9.7; 11.6; -7.3; -7.4; -7.8; -36.6
SECONDARY
Erythema, Scaling and Induration Scores at Each Visit
2.0; 2.0; 2.6; 2.5; 2.6; 2.5
SECONDARY
Percent Changes of Erythema, Scaling and Induration From Day 1 to Day 19
-0.0; 0.1; -0.1; -0.1; -3.0; -1.0
SECONDARY
Number of Participants With Success Rate at Each Visit
0; 0; 0; 0; 0; 0
SECONDARY
Time to First Success
23; 23; 24; 23; 23; 15

Summary

This was an exploratory, single-center, investigator blinded, randomized, controlled, intra-individual study, involving participants with psoriasis vulgaris. The objective was to evaluate, in a modified Dumas-Scholtz psoriasis mini-zone test, the safety and efficacy of CD10367 solution at 1% and 3% after a 3-week treatment period of once daily application.

Eligibility Criteria

Inclusion Criteria

  • Adult male or female aged at least 18 and up to 70 years old inclusive at screening visit.
  • Female of non childbearing potential (postmenopausal [absence of menstrual bleeding for 1 year prior to screening, without any other medical reason], hysterectomy or bilateral oophorectomy).
  • Participant had a skin phototype I to IV on Fitzpatrick's scale. (Screening visit).
  • The participant had a clinical diagnosis of stable plaque psoriasis, defined as no flare during the month before Screening visit and no change between Screening visit and Baseline visit, of mild to moderate severity. (Screening visit and Baseline Visit).
  • The participant presented with at least six eligible mini-zones, on at least two psoriasis plaques (Screening visit and verified also at Baseline Visit) with specific severity grades,
  • Participant agreed not to wear his/her contact lenses from the Baseline visit till the D19 visit (Screening visit).

Exclusion Criteria

  • The participant presented guttate, erythrodermic, exfoliative, inverse, pustular, palmo plantar, infected or ulcerated psoriasis (Screening visit).
  • The participant had any uncontrolled or serious disease, or any medical or surgical condition, that might either interfere with the interpretation of the clinical trial results, and/or put the participant at significant risk (according to Investigator's judgment) if he/she participated in the clinical trial (e.g. history of on-going gastric or duodenal ulcer, clinically significant lung disease, etc.) (Screening visit).
  • The participant had known or suspected allergies or sensitivities to any components of the study drugs or of the keratolytic product (see Investigator's Brochure/Product label). (Screening visit).
  • The participant had known history of adverse drug reaction or hypersensitivity to a product with the same mode of action.
  • The participant had any abnormal clinically significant findings according to the ophthalmologist, at the ophthalmological exam at Screening visit,
  • The participant presented any abnormal laboratory tests judged clinically significant by the investigator (blood samplings and urinalysis done at Screening visit),
  • The participant had QTc interval >450 millisecond (msec) or any abnormal electrocardiogram (ECG) value considered as clinically significant by the cardiologist (Screening visit).
  • The participant had received, applied or taken some specified treatments within the specified time frame prior to the Baseline visit.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03025282). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search