A Multiple Dose Study Of PD-0360324 In Patients With Active Cutaneous Lupus Erythematosus
- Disease/Condition
- Cutaneous Lupus Erythematosus
- Drug/Device/Intervention
- PD-0360324
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Pfizer
- Location
- Anniston,Oxford,Los Angeles,Orange Park,Chicago,Indianapolis,Fort Gratiot,Charlotte,Ducansville,Philadelphia,Wyomissing,Rapid City,Rapid City,Jackson,Dallas,Norfolk,Clarksburg,Markham,Chisinau, Canada,Moldova - Republic of,United States of America
- Phase
- Phase 1
- Start date
- Nov 01, 2011
- End date
- Nov 01, 2013
- Enrollment
- 28 participants
Safety and tolerability of PD- 0360324 will be assessed by physical examinations, adverse event and infection monitoring, 12 lead ECGs, vital sign, and clinical safety laboratory measurements.
This study is designed to evaluate the safety and tolerability of multiple intravenously
 administered doses of PD-0360324 in patients with cutaneous lupus erythematosus. Changes in
 disease activity will also be evaluated.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT01470313
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT01470313 through Pure Global AI's free database. This Phase 1 trial is sponsored by Pfizer and is currently Terminated. The study focuses on Cutaneous Lupus Erythematosus. Target enrollment is 28 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.