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Phase I/II Trial Involving Preterm Neonates

A Rare Disease Case Study

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About the Case Study

Pharm-Olam was contracted to provide clinical research services on a Phase I/II pediatric Respiratory Distress Syndrome study involving neonates with a gestational age between 27 and 33 weeks. This first in-human study required a single intratracheal administration within 24 to 48 hours of birth.

Discover the challenges Pharm-Olam encountered and the solutions implemented in this pediatric study.

Sites & Locations:
12 sites in 3 countries - Great Britain, Germany, and Czech Republic


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