
Method Comparison of the ChemDx Acetylcholinesterase Test System In Prescription Home-Use and Professional CLIA-Waived Settings versus EQM Test-mate™
Primary Coordinator: Jack Wisman (Jack@proc211.com)

Phase 3, multicenter, randomized, double-blind, group sequential, placebo-controlled study to assess efficacy and safety of rimegepant for the treatment of migraine (with or without aura) in children and adolescents ≥ 6 to <18 years of age
For more info: https://clinicaltrials.gov/study/NCT04649242
Primary Coordinator: Uyen Tran (Uyen@proc211.com)

Phase 3, multicenter, open-label study to assess the long-term safety and tolerability of rimegepant for the acute treatment of migraine (with or without aura) in children and adolescents ≥ 6 to <18 years of age
For more info: https://clinicaltrials.gov/study/NCT04743141?id=C4951003&rank=1
Primary Coordinator: Uyen Tran (Uyen@proc211.com)

Phase 3 Randomized, Multi-Center, Placebo-Controlled, Masked Study to Evaluate the Clinical Efficacy and Safety of Fucithalmic® (Fusidic Acid 1%) Viscous Topical Antibiotic Eye Drops for the Treatment of Suspected Bacterial Conjunctivitis
For more info: https://clinicaltrials.gov/study/NCT06911424
Primary Coordinator: Jack Wisman (Jack@proc211.com)

Phase 2, Randomized, Double-Blind, Active-Controlled, Dose-Finding Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-31 in Healthy Infants Given 4 Doses at 2, 4, 6, and 12–15 Months of Age Concomitantly with Routine Pediatric Vaccines
For more info:
Primary Coordinator: Cathy Hansa (Catherine@proc211.com)

Phase 1, Randomized, Double-Blind, Active Comparator Controlled Study to Evaluate the Safety, Tolerability, and Immunogenicity of a Novel Pneumococcal Vaccine in Children
Primary Coordinator: Cathy Hansa (Catherine@proc211.com)

Phase 2, Randomized, Double-Blind Trial to Evaluate the Safety, Tolerability, and Immunogenicity of a Multivalent Pneumococcal Conjugate Vaccine in Healthy Infants
Primary Coordinator: Uyen Tran (Uyen@proc211.com)
For more info:
https://www.pfizerclinicaltrials.com/nct06524414-pneumococcal-disease-trial

Primary Coordinator: Cathy Hansa (Catherine@proc211.com)
For more info:
See our RSV study information tab for more information!

Phase 3 protocol to investigate the safety, tolerability, and immunogenicity of a BNT152b2 (LP.8.1) -- Adapted vaccine in children 5 through 11 years of age considered at high risk for severe COVID-19
Primary Coordinator: Uyen Tran (Uyen@proc211.com)
For more info:
https://clinicaltrials.gov/study/NCT07222384

Phase 2, Randomized, Double-Blind, Active-Controlled, Dose-Finding Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-31 in Healthy Infants Given 4 Doses at 2, 4, 6, and 12–15 Months of Age Concomitantly with Routine Pediatric Vaccines
Primary Coordinator: Cathy Hansa (Catherine@proc211.com)
For more info:
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