Pediatric Research of Charlottesville
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Pediatric Research of Charlottesville
Home
Our Studies
About Us
Contact Us
In The News
RSV Study Information
More
  • Home
  • Our Studies
  • About Us
  • Contact Us
  • In The News
  • RSV Study Information

  • Home
  • Our Studies
  • About Us
  • Contact Us
  • In The News
  • RSV Study Information

Enrolling! Contact a study coordinator with questions

Method Comparison of the ChemDx Acetylcholinesterase Test System

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)


Pfizer Rimegepant Migraine Treatment

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)


Pfizer Long-term Migraine Treatment

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)

Baxis Fucithalmic Topical Antibiotic Eye Drops for treatment of Bacterial Conjunctivitis

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)

Vaxcyte 31-Valent Pneumococcal Conjugate Vaccine

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:

https://clinicaltrials.gov/study/NCT06720038?locStr=Charlottesville,%20VA&country=United%20States&state=Virginia&city=Charlottesville&cond=pneumococcal%2031&rank=2&tab=table


Primary Coordinator: Cathy Hansa (Catherine@proc211.com)



Enrolling soon!

Merck Sharpe & Dohme's Pneumoccocal Vaccine

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)

 


Studies Currently in Follow-Up

Pfizer 25-Valent Pneumococcal Conjugate Vaccine

Pfizer 25-Valent Pneumococcal Conjugate Vaccine

Pfizer 25-Valent Pneumococcal Conjugate Vaccine

 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

Sanofi RSV Vaccine for Infants and Toddlers

Pfizer 25-Valent Pneumococcal Conjugate Vaccine

Pfizer 25-Valent Pneumococcal Conjugate Vaccine

Primary Coordinator: Cathy Hansa (Catherine@proc211.com)


For more info:

https://clinicaltrials.gov/study/NCT06252285?cond=Respiratory%20Syncytial%20Virus&intr=Vaccine&term=Sanofi&rank=8


See our RSV study information tab for more information!

Pfizer Open label COVID-19 Vaccine in Children High Risk for Severe COVID-19

 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


Vaxcyte 31-Valent Pneumococcal Conjugate Vaccine

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:

https://clinicaltrials.gov/study/NCT06720038?locStr=Charlottesville,%20VA&country=United%20States&state=Virginia&city=Charlottesville&cond=pneumococcal%2031&rank=2&tab=table




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