On February 27, join Johnson & Johnson Innovation – JLABS afternoon programme on "Road to First-in-Human Trials for Biologics"
Are you a biotech startup eager to navigate the complex landscape of first-in-human clinical trials for biologics? JLABS upcoming program is designed to equip you with valuable insights needed to understand and prepare for this critical phase of large molecule drug development. As competition for funding is fierce, startups are expected to demonstrate a clear blueprint for their clinical trials strategy, and we want you to be ready.
Large molecule biologics often have unique characteristics that may require specialized procedures. Understanding and navigating these pathways while ensuring compliance with stringent and ever-changing regulations can be challenging. How do you adapt your trials strategy to current market conditions?
The programme will investigate four topics in detail:
- Topic 1: Preclinical Development strategies
During this session the speakers will discuss the groundwork necessary before advancing to clinical trials, including toxicity, drug metabolism & pharmacokinetics.
- Topic 2: Chemistry, Manufacturing & Controls (CMC)
The discussion will focus on the complexities of CMC to ensure your biologics manufacturing processes and quality control measures meet regulatory standards. This includes optimizing the manufacturing of your Active Pharmaceutical Ingredient (API) and drug product formulations.
- Topic 3: Clinical Trial Designs
The speakers will explore strategies for designing effective clinical trials specific to biologics, with a focus on demonstrating safety and laying the groundwork for demonstrating efficacy. Topics include operational aspects such as clinical trial site recruitment and patient enrollment.
- Topic 4: Regulatory Strategies
During this session the speakers will elaborate on the European regulatory landscape, focusing on Clinical Trial Application requirements for your First-in-Human trial.
Learn more about the programme and register here.
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