Release Date: November 05, 2024
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
Q: What are the specific parameters MacroGenics needs to see from the data next year to decide on the future of vobra duo? A: Scott Koenig, President and CEO, stated that they are close to obtaining final data and are monitoring patients post-dosing. They will assess the final rPFS, safety profile, competitive landscape, and other portfolio factors. Specific parameters for decision-making will be shared in the coming months.
Q: Can you provide details on the search process for the next CEO and the timeline for the transition? A: Scott Koenig mentioned that a Board subgroup has been selected to initiate the search process with an outside firm. He will remain in his role until a new CEO is selected, ensuring a smooth transition. The process is expected to take a few months.
Q: How is the Phase 1 dose escalation for MGC026 progressing, and when can investors expect initial clinical data? A: Scott Koenig reported that the dose escalation is progressing well, with expectations to complete the study in 2025 and report data within the same year.
Q: What triggered the decision to pause the lorigerlimab and vobra duo combination study? A: Scott Koenig explained that they are awaiting final TAMARACK data to assess the appropriate vobra dose before continuing with combination studies. The decision was made to ensure the best dose is used moving forward.
Q: Are there any notable differences in the safety profiles of vobra duo and MGC026? A: Scott Koenig noted that distinct safety profiles are expected due to different mechanisms of action. However, it is too early to provide a side-by-side comparison as MGC026 is still in the middle of dose escalation.
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
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