Sentinel lymph node working group data acquisition project,
Role: Investigator,
University of California, San Francisco,
(02/2026 - 02/2027)
Status: Approved
For Profit Organization
A phase 3, open-label study of the safety, efficacy, and tolerability of apomorphine administered by continuous subcutaneous infusion in advanced Parkinson's disease patients with unsatisfactory control on available therapy,
Role: Investigator,
U.S. World Meds,
(11/2021 - 11/2022)
Status: Completed
A multi-center, open registry of patients with psoriasis who are candidates for systemic therapy including biologics,
Role: PI,
Jansseen Biotech, Inc.,
(09/2020 - 09/2021)
Status: Completed
A prospective observational study of patients receiving Dupixent for Atopic Dermatitis,
Role: PI,
Regeneron Pharmaceuticals, Inc.,
(03/2020)
Status: Approved
A multi-center, epidemiology study to evaluate the potential for adverse health effects in fetuses and live-born infants following a woman's pregnancy, compared with a similar group of psoriatic women not exposed to tazarotene and compared with background levels in general population.,
Role: PI,
Allergan Inc.,
(01/2006 - 01/2007)
Status: Completed
A multi-center study to assess the impact of topical corticosteriods on the safety and efficacy of protopic (tacrolimus) ointment in the short-term treatment of atopic dermatitis and to assess protopic in the long-term management of atopic dermatitis,
Role: PI,
Fujisawa,
(10/2005 - 10/2006)
Status: Completed
Open-label study to evaluate the use of imiquimod 5% topical cream for reducing postsurgical recurrence or persistence of Basal Cell Carcinoma following excision by Curettage,
Role: Investigator,
3M Pharmaceuticals,
(10/2005 - 10/2006)
Status: Completed
Tazorac (Tazarotene topical gel 0.1%) observation study in stable plaque psoriasis on up to 20% body surface,
Role: PI,
Allergan Inc.,
(09/1998 - 09/1999)
Status: Completed
A Double-Blind, Randomized Study to Assess the Quality of Life and Cost of Disease in Patients with Herpes Zoster Treated with Famciclovir or Placebo,
Role: Investigator,
Smithkline Beecham,
(06/1995 - 06/1996)
Status: Completed
A clinical study evaluating the safety and efficacy of Tazorac gel compared with Dovonex 0.005% ointment in the treatment of individuals with stable plaque psoriasis,
Role: PI,
Allergan Inc.,
Status: Completed
A 6 month, randomized, multicenter, parallel-group, double-blind, vehicle-controlled study to evaluate the efficacy and safety of ASM 981 (primecrolimus) cream 1% BID vs standard of care in management of mild to severe atopic dermatitis in children 3 months to 11 years,
Role: PI,
Novartis Pharma AG,
Status: Completed
A Phase IIIb, open-label, multicenter study to evaluate the safety of 1.0 mg/kg subcutaneously administered Efalizumab in adults with moderate to severe plaque psoriasis, including those who are receiving concomitant antipsoriatic therapies or have recently transitioned from systemic therapies,
Role: PI,
Genentech, Inc.,
Status: Completed
Internal
A Comparison Between Cryosurgery Alone, Cryosurgery Plus Interferon, and Interferon Alone in the Treatment and Long-Term Recurrence of Condyloma Acuminata,
Role: PI,
LLU Dept. of Medicine,
Status: Completed