Suleyman Eralp al Bellibas

Advisory Board Member @Iq Consortium

East Hanover, NJ, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Oct 2024 — Present

Advisory Board Member @Iq Consortium

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DC, US

Novartis representative for Clinical Pharmacology Leadership Group in IQ Consortium

EDUCATION

N/A

Ege University

PhD Eq., Medical Pharmacology

1990 — 1991

Università degli Studi di Milano

Fellow, Medical Pharmacology

N/A

NATO ASI Erice International School of Pharmacology

New Trends in Pharmacokinetics; Pharmacovigilance

1997 — 1999

University of California, San Francisco

MSD International fellow, Postdoc, Clinical Pharmacology

N/A

Ankara University

Doctor of Medicine (M.D.), Medicine

SKILLS

BiomarkersRegulatory SubmissionsDrug MetabolismTherapeutic AreasPharmacologyPharmaceuticalsIndBiologicsAnti-InfectivesRegulatory AffairsLifesciencesPhase IAlzheimer's DiseaseClinical ResearchClinical PharmacologyPk PdBiotechnologyPharmaceutical ResearchAtherosclerosisProduct Life Cycle ManagementOncologyProtocolNdaCardiovascular MedicineTranslational ResearchImmunologyDue DiligenceMedical WritingPharmacokineticsPharmacodynamicsClinical DevelopmentNeurosciencePharmaceutical IndustryFdaNeuropharmacologyDrug SafetyTranslational MedicineCholesterolVirologyCRO

ABOUT SULEYMAN ERALP AL BELLIBAS

Physician-Scientist/Pharmaceutical/Biotech R&D Executive/Translational Medicine/Clinical Pharmacology Subject Matter Expert/Drug Developer with an exceptional track record in Early Development for Adult and Pediatric Indications-20+ years of innovation experience in the US and Global pharmaceutical/biotech industry (Roche, Johnson & Johnson, Novartis, The Medicines Company, Former VP at Parexel)- Postdoc training at UCSF as MSD International Fellow in Clinical Pharmacology- Fellow of the American Heart Association- Scientific Advisor for INDdose, a smartphone app to calculate estimated maximum safe starting dose in First in Human clinical trials- Early Phase Drug Development/Translational Medicine/Clinical Pharmacology Expertise for Small Molecules and Biologics- Contributed development activities of 100+ NMEs at various phases of development ranging from IND/Phase 1 to NDA and Global Registration trials- Co-developer 6 successfully filed and approved first in class NDAs- Fuzeon®: First in class HIV fusion inhibitor drug. Approved for Adult and Pediatric indications in less than two years of clinical development time-Exelon Patch®: First transdermal therapeutics for Alzheimer’s Dementia-Orbactiv®: First single-dose antibiotic for Skin and Skin structure infections-Kengreal®: First and only intravenous P2Y12 antiplatelet agent approved as an adjunctive therapy to percutaneous coronary intervention (PCI) for reducing periprocedural thrombotic events-Leqvio®: First in class siRNA PCSK9 inhibitor to lower cholesterol-Fabhalta®: First in class Factor B inhibitor for several rare immunology/hematology/nephrology indications.

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Suleyman Eralp al Bellibas — Advisory Board Member at Iq Consortium in East Hanover, NJ, US | Unifers