HomeTrialNCT06780332
🔬NCT06780332Phase 4ACTIVE NOT RECRUITING

Rapid Drug Desensitization Study in Adults Experiencing Hypersensitivity Reactions to Palynziq

Study Summary

The purpose of this study is to determine if rapid drug desensitization (RDD) to Palynziq will improve drug tolerability and treatment persistence in adult patients on commercial Palynziq experiencing hypersensitivity reactions (HSRs) leading to treatment interruption or reduction of dose or dosing frequency. See Section 10.8 for full list of HSR preferred terms. Study details include: * Study duration: Up to 30 weeks (up to 6 weeks for Screening, then RDD, and 24 weeks of follow-up) * RDD duration: 1 day * Palynziq dosing/follow-up duration: 24 weeks * Palynziq dosing frequency: Individualized

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment9 participants
Primary Completion
Lead SponsorBioMarin Pharmaceutical
Data Retrieved2026-04-11 02:55:23.531335+00:00
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