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023
FDA & EMA Regulatory Recommendations on Fed Bioequivalence Study in Healthy Subjects vs Patients for Generic Drug Development
Sunday, September 8, 2024
5:00 PM – 7:00 PM
ET
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166
Fetal & Neonatal Drug Exposure Following Nipocalimab Treatment in Pregnant Women at Risk of EOS-HDFN
Monday, September 9, 2024
5:00 PM – 7:00 PM
ET
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061
First-in-Human Evaluation of Pharmacokinetics & Safety of Tilpisertib Fosmecarbil, an Oral Prodrug of a Tumor Progression Locus 2 Inhibitor, in Healthy Volunteers
Sunday, September 8, 2024
5:00 PM – 7:00 PM
ET
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076
First-in-Human Phase 1 SAD, MAD, Food Effect & DDI Study of SGR-1505, a Mucosa-Associated Lymphoid Tissue Lymphoma Translocation Protein 1 Inhibitor, in Healthy Volunteers
Sunday, September 8, 2024
5:00 PM – 7:00 PM
ET
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055
First-in-Human Population PKPD Modelling & Simulation of CUE-101: Preliminary Results
Sunday, September 8, 2024
5:00 PM – 7:00 PM
ET
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106
First-in-Human Safety, Pharmacokinetics & Pharmacodynamics of the Oral Factor D Inhibitor BCX10013
Monday, September 9, 2024
5:00 PM – 7:00 PM
ET
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128
Food & Formulation Effect of a Novel Src Homology Region 2 Domain−containing Protein Tyrosine Phosphatase 2 (SHP2) Allosteric Inhibitor in Combination With Pembrolizumab
Monday, September 9, 2024
5:00 PM – 7:00 PM
ET