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PRG 1801
PRG 1801
PRG 1801
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PRG-1801 has received IND clearance by • Modified structure complying with FDA safety requirement
NMPA for clinical trail and is filing in FDA • Lentivirus with Serum-free culture
Strong safety database in MM indication • Sophisticated IPR protection
Low levels of CRS • Shrank tumors in nearly 88% of relapsed multiple myeloma
Distinct MOA to other CAR-Ts patients and eliminated them in 56%
Integrated R&D platform: PRG CGT + Rational for the development of PRG-1801 for MM
Naffibody Platform 1. Anti-BCMA VHH specifically designed for CAR-T
- High specificity and affinity
- Less cross-pairing effect
2. Stable manufacturing with low cost
- Optimized plasmid design
- Stable and high-yield vector production system.
- Self-developed QC methods with low cost
3. Superior clinical safety and efficacy
- Low frequence and severity of AE
- Long duration of efficacy