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Dermacyd PH_DETINLYN

Phase 3

Undisclosed | Small molecule | Other |Sanofi|Trials Updated: Aug 25, 2009

Dermacyd PH_DETINLYN target and mechanism

ModalitySmall molecule

Also known as Dermacyd PH_DETINLYN (Lactic Acid)

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials3
Total Enrollment132

FDA Designations

No designations recorded

Dermacyd PH_DETINLYN clinical trials

Dermacyd PH_DETINLYN · 3 trials · 1 indication

Phase 3 3
NCT00785590Dermacyd PH_DETINLYN (Lactic Acid) Sweet Flower - Photo Evaluation.Hygiene
COMPLETED26 Analytics
NCT00785655Dermacyd PH_DETINLYN (Lactic Acid) Sweet Flower - CompatibilityHygiene
COMPLETED53 Analytics
NCT00786097Dermacyd PH_DETINLYN (Lactic Acid) Tangerine Mix - CompatibilityHygiene
COMPLETED53 Analytics
PHASE3COMPLETED
Dermacyd PH_DETINLYN (Lactic Acid) Sweet Flower - Photo Evaluation.
HygieneUnlock trial analytics
PHASE3COMPLETED
Dermacyd PH_DETINLYN (Lactic Acid) Sweet Flower - Compatibility
HygieneUnlock trial analytics
PHASE3COMPLETED
Dermacyd PH_DETINLYN (Lactic Acid) Tangerine Mix - Compatibility
HygieneUnlock trial analytics

Study Endpoints

Primary Endpoints

The photo irritation test and the photosensitivity will be measured using UVA irradiation and evaluated according International Contact Dermatitis Research Group (ICDRG) scale
Throughout the study
The sensibility will be evaluated according to the skin type.
Throughout the study
The absence of primary and accumulated dermical irritability and dermical sensitivity will be evaluated using International Contact Dermatitis Research Group (ICDRG) scale.
Throughout the study
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeSUPPORTIVE_CARE

Treatment Arms

ArmTypeDescription
1EXPERIMENTALDermacyd PH\_DETINLYN (Lactic Acid)

Interventions

NameTypeDescription
Dermacyd PH_DETINLYN (Lactic Acid)DRUG -
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Eligibility Criteria

Age Range18 Years to 60 Years
SexFEMALE
Healthy VolunteersYes
Study Sites1

Inclusion criteria: * Phototype Skin II and III; * Integral skin test in the region; * Willingness in following the study procedures and to be present in the clinic at the days and scheduled time for medical evaluations and for application of occlusion; Exclusion criteria: * Lactation or gestatio...

Countries:Brazil
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Frequently asked questions about Dermacyd PH_DETINLYN

What is Dermacyd PH_DETINLYN?

Dermacyd PH_DETINLYN is a small molecule product developed by Sanofi, known in full as Dermacyd PH_DETINLYN (Lactic Acid). It has been studied in Phase 3 clinical trials in the hygiene area, specifically in Brazil, in studies enrolling healthy adult female volunteers aged 18 years and older.

Who makes Dermacyd PH_DETINLYN?

Dermacyd PH_DETINLYN is developed by Sanofi, which trades under the ticker SNY. Sanofi sponsored the Phase 3 clinical program for the product, including the compatibility and photo evaluation studies conducted in Brazil.

What phase is Dermacyd PH_DETINLYN in?

Dermacyd PH_DETINLYN has been studied in Phase 3 clinical trials. Three Phase 3 studies have been completed, and none are currently active. The program enrolled a total of 132 participants across those completed trials.

What clinical trials is Dermacyd PH_DETINLYN in?

Dermacyd PH_DETINLYN has been evaluated in three completed Phase 3 trials: NCT00786097, a Tangerine Mix compatibility study enrolling 53 participants; NCT00785655, a Sweet Flower compatibility study enrolling 53 participants; and NCT00785590, a Sweet Flower photo evaluation study enrolling 26 participants. All were conducted in Brazil.

Is Dermacyd PH_DETINLYN the same as lactic acid?

Dermacyd PH_DETINLYN is also known as Dermacyd PH_DETINLYN (Lactic Acid), reflecting lactic acid as the named component. Searches for either name refer to the same Sanofi product studied in the Phase 3 hygiene trials.

What is Dermacyd PH_DETINLYN used for?

Dermacyd PH_DETINLYN has been studied in the hygiene therapeutic area. Its Phase 3 trials were conducted in healthy adult female volunteers aged 18 years and older in Brazil, evaluating compatibility and photo evaluation endpoints rather than a disclosed disease indication.