Healthcare/Biotech Analysts discuss Jasper Therapeutics’ FDA clearance for their Investigational New Drug (IND) application for a dose escalation Phase Ib/IIa study of its CD117 (c-KIT) targeted antibody briquilimab in chronic spontaneous urticaria (CSU) on an Analyst/Industry conference call to be held on October 11 at 8 am.
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Read More on JSPR:
- William Blair healthcare/biotech analysts hold analyst/industry conference call
- Jasper Therapeutics to Host Key Opinion Leader Webinar on the Potential of Briquilimab for Chronic Urticaria on October 11, 2023
- Jasper Therapeutics Announces IND Clearance for Phase 1b/2a Study of Subcutaneous Briquilimab in Chronic Spontaneous Urticaria
- Jasper receives IND clearance for Phase 1b/2a study of subcutaneous briquilimab
- Jasper Therapeutics appoints Herb Cross CFO
