Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Allogeneic NK Cells · 1 trial · 9 indications
Dose Limiting toxicities assessed in a incrementing dose design.
| Arm | Type | Description |
|---|---|---|
| AlloNK | EXPERIMENTAL | AlloNK, dosed after a conditioning regimen, combined with Rituximab. |
| Name | Type | Description |
|---|---|---|
| Allogeneic NK Cells | DRUG | AlloNK, dosed after a conditioning regimen, combined with Rituximab. |
For Subjects with Refractory Rheumatoid Arthritis (RA): * Documented diagnosis of RA, meeting the 2010 ACR/EULAR classification criteria. * Rheumatoid Factor (RF) or Anti Citrullinated Protein Antibody (ACPA) positive. * High-sensitivity C-reactive protein (hs-CRP) \> 3 mg/L or Erythrocyte Sediment...
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