Dermatitis
📧 Sign up to get email alerts when something new happens for Dermatitis.
Sign up freeTop drugs studied for this disease
-
CLINICAL_TRIALS trial_result · 2019-04-05Clinical Trial Update: Study of Epigallocatechin-3-gallate (EGCG) for Skin Prevention in Patients With Breast Cancer Receiving Adjuvant Radiotherapy [Phase 2]
Phase 2 trial evaluating epigallocatechin-3-gallate (EGCG) for skin prevention in breast cancer patients undergoing adjuvant radiotherapy.
-
FDA approval · 2019-02-21FDA Approved: PREDNISONE — Supplemental Application (Mylan Pharmaceuticals Inc.)
The FDA approved a supplemental application for prednisone from Mylan Pharmaceuticals, indicating approval of an existing generic product's …
-
FDA approval · 2019-01-30FDA Approved: DESONIDE OINTMENT, 0.05% — Original Application (Encube Ethicals, Inc.)
FDA approved Desonide Ointment 0.05% as a generic topical corticosteroid for relief of inflammatory and pruritic skin conditions; indicated …
-
FDA approval · 2018-12-26FDA Approved: CLOBETASOL PROPIONATE — Original Application (AvKARE)
FDA approved AvKARE's original ANDA for clobetasol propionate topical product (generic).
-
FDA approval · 2018-12-14FDA Approved: HYDROCORTISONE VALERATE — Original Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved Glenmark's hydrocortisone valerate as a generic topical corticosteroid under an original ANDA (ANDA211750).
- Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
-
FDA approval · 2018-11-29FDA Approved: FLUOCINONIDE — Original Application (Encube Ethicals, Inc.)
The FDA approved Encube Ethicals, Inc.'s fluocinonide topical solution 0.05% as a generic topical corticosteroid for inflammatory and prurit…
-
FDA approval · 2018-11-08FDA Approved: NYSTATIN AND TRIAMCINOLONE ACETONIDE — Original Application (Viona Pharmaceuticals Inc)
The FDA approved the original application for a generic topical cream containing nystatin and triamcinolone acetonide, manufactured by Viona…
-
FDA approval · 2018-10-16FDA Approved: FLUOCINONIDE — Original Application (Encube Ethicals, Inc.)
FDA approved Fluocinonide under Encube Ethicals, Inc.'s Original Application (ANDA 211410), establishing regulatory approval for this topica…
-
FDA approval · 2018-10-12FDA Approved: BETAMETHASONE DIPROPIONATE — Original Application (Cosette Pharmaceuticals, Inc.)
The FDA approved Cosette Pharmaceuticals' original application for a generic Betamethasone Dipropionate topical product.
-
FDA approval · 2018-10-04FDA Approved: CLOBETASOL PROPIONATE — Original Application (Taro Pharmaceuticals U.S.A., Inc.)
FDA approved CLOBETASOL PROPIONATE as an original-application generic topical product. The approval holder is Taro Pharmaceuticals U.S.A., I…
-
FDA approval · 2018-08-21FDA Approved: FLUOCINONIDE CREAM — Original Application (Amneal Pharmaceuticals NY LLC)
FDA approved a generic fluocinonide cream from Amneal Pharmaceuticals NY LLC (ANDA 210554).
-
FDA approval · 2018-07-17FDA Approved: FLUOCINONIDE — Original Application (Zydus Lifesciences Limited)
FDA approved the fluocinonide topical product from Zydus Lifesciences Limited via an Original Application, marking the first generic entry f…
-
FDA approval · 2018-06-27FDA Approved: METHYLPREDNISOLONE ACETATE — Original Application (Sagent Pharmaceuticals)
The FDA approved the original application for methylprednisolone acetate from Sagent Pharmaceuticals, enabling a generic topical corticoster…
-
CLINICAL_TRIALS research · 2018-05-31Clinical Trial Update: Treatment of Incontinence Associated Dermatitis - Automated [NA]
This entry provides an update on a clinical trial evaluating an automated treatment for incontinence-associated dermatitis, including urinar…
-
CLINICAL_TRIALS research · 2018-05-30Clinical Trial Update: Maintaining Lower Levels of Care Through Automated Perineal Hygiene [NA]
This clinical trial update reports on an automated perineal hygiene system intended to maintain lower levels of care for individuals with ur…
-
FDA approval · 2018-04-23FDA Approved: FLUOCINONIDE — Original Application (NorthStar RxLLC)
FDA approved Fluocinonide through an Original Application (generic) submitted by NorthStar RxLLC.
-
CLINICAL_TRIALS research · 2018-04-10Clinical Trial Update: Interest of Photographs by Smartphone in Dermatology
A ClinicalTrials.gov update examines the use of smartphone photographs in dermatology, with dermatitis as the condition. The trial status is…
-
FDA approval · 2018-03-28FDA Approved: DIPROLENE — Supplemental Application (Organon LLC)
FDA approved a supplemental application for Diprolene (betamethasone dipropionate) from Organon LLC.
-
FDA approval · 2018-03-16FDA Approved: DESOXIMETASONE — Original Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' desoximetasone topical product under an original application, enabling a generic version of this topical…
-
FDA approval · 2018-01-30FDA Approved: CLOBETASOL PROPIONATE — Original Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' generic clobetasol propionate topical as an Original Application (ANDA). It is indicated for inflammator…
-
FDA approval · 2017-11-21FDA Approved: HYDROCORTISONE BUTYRATE — Original Application (The J. Molner Company LLC)
The FDA approved a generic topical hydrocortisone butyrate product under an Original Application (ANDA 209556) from The J. Molner Company LL…
-
CLINICAL_TRIALS trial_result · 2017-11-06Clinical Trial Update: Black Tea Compresses for Facial Eczema and Perioral Dermatitis [NA]
A completed clinical trial evaluated the use of black tea compresses for facial eczema and perioral dermatitis.
-
CLINICAL_TRIALS trial_result · 2017-11-01Clinical Trial Update: Micro-Technique Sampling
A Kimberly-Clark-sponsored clinical trial evaluating micro-technique sampling for dermatitis has completed.
-
FDA approval · 2017-10-27FDA Approved: CLOBETASOL PROPIONATE — Original Application (Zydus Pharmaceuticals USA Inc.)
FDA approved the original ANDA for a generic clobetasol propionate topical product from Zydus Pharmaceuticals USA Inc.
-
FDA approval · 2017-09-19FDA Approved: DESOXIMETASONE — Original Application (Viona Pharmaceuticals Inc)
FDA approved Desoximetasone from Viona Pharmaceuticals Inc via an Original Application (ANDA205206).