Determine Pharming Group NV go-to-market proposition and gain insight into the company’s clinical operations, recruitment, and trial strategy.
|Trial Title||Trial Identifier||Drug Name||Therapy Area||Indication||Trial Phase||Trial Status||Sponsor|
|Deserunt mollit sunt Lorem||GDCTXXXX||Lorem||Lorem||Lorem||XXXX||Planned||Pfizer Inc|
|Pediatric Patients Aged 4 to 11 Years With APDS||GDCT0459793||leniolisib||Genetic Disorders||PASLI Disease (Activated PI3K Delta Syndrome (APDS))||Phase III||Planned||Pharming Technologies BV|
|Recombinant Human C1 Esterase Inhibitor (Conestat Alfa) in the Prevention of Acute Ischemic Cerebral and Renal Events After Transcatheter Aortic Valve Implantation (PAIR-TAVI)||GDCT0441424||conestat alfa||Cardiovascular; Genito Urinary System And Sex Hormones||Acute Ischemic Stroke; Acute Renal Failure (ARF) (Acute Kidney Injury)||Phase II||Ongoing, recruiting||University Hospital Basel|
|A Pediatric Clinical Study of Leniolisib||GDCT0438900||leniolisib||Genetic Disorders; Oncology||Angioimmunoblastic T-Cell Lymphoma (AITL)/Immunoblastic Lymphadenopathy; PASLI Disease (Activated PI3K Delta Syndrome (APDS))||Phase II/III||Planned||Pharming Group NV|
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