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Senti Bio Announces FDA Clearance of IND Application for SENTI-202 for the Treatment of Relapsed or Refractory Hematologic Malignancies Including Acute Myeloid Leukemia

– First patient in Phase 1 clinical trial expected to be treated in Q2 2024 – – Initial clinical efficacy data expected by year-end 2024 and durability data expected in 2025 – –. ....

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Senti Biosciences, Inc.: Senti Bio Announces FDA Clearance of IND Application for SENTI-202 for the Treatment of Relapsed or Refractory Hematologic Malignancies Including Acute Myeloid Leukemia

Senti Biosciences, Inc.: Senti Bio Announces FDA Clearance of IND Application for SENTI-202 for the Treatment of Relapsed or Refractory Hematologic Malignancies Including Acute Myeloid Leukemia
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Senesco Technologies (SNTI) Announces FDA Clearance of IND Application for SENTI-202

Senesco Technologies (SNTI) Announces FDA Clearance of IND Application for SENTI-202
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Senti Bio Announces Multiple Data Presentations at the Society for Immunotherapy of Cancer Annual Meeting

– Two poster presentations highlighting new preclinical data with BlueRock Therapeutics – – Two poster presentations showcasing Senti Bio’s proprietary Gene Circuit platform – SOUTH SAN. ....

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Senti Bio Announces Multiple Data Presentations at the

– Two poster presentations highlighting new preclinical data with BlueRock Therapeutics – – Two poster presentations showcasing Senti Bio’s proprietary. ....

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