Compassionate Use of Dupilumab for Adult Patients With Bullous Pemphigoid

NCT05906706 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2025-07-03

No results posted yet for this study

Summary

The objective of the program is to provide patients with Bullous Pemphigoid (BP), that participated in the R668-BP-1902 (NCT04206553) phase 2/3 study, dupilumab treatment and evaluate the long-term safety of dupilumab.

Conditions

  • Bullous Pemphigoid

Interventions

DRUG

dupilumab

Subcutaneous (SC) administration

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05906706 on ClinicalTrials.gov