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| Inactive Indication- | 
| Drug Highest PhasePreclinical | 
| First Approval Ctry. / Loc.- | 
| First Approval Date20 Jan 1800 | 
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| Drug Highest PhasePreclinical | 
| First Approval Ctry. / Loc.- | 
| First Approval Date20 Jan 1800 | 
 / Not yet recruitingPhase 1/2 A Phase 1 and 2a open-label study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity and antitumor activity of LAVA-051 in patients with relapsed or refractory CD1d-positive chronic lymphocytic leukemia, multiplemyeloma or acute myeloid leukemia - LAVA
| Start Date28 Dec 2021 | 
| Sponsor / Collaborator- | 
A Phase 1 Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity and Antitumor Activity of LAVA-051 in Patients with Relapsed or Refractory CLL, MM, or AML
A phase 1, first-in-human trial to evaluate the safety and tolerability of LAVA-051 in patients with relapsed or refractory Chronic Lymphocytic Leukemia (CLL), Multiple Myeloma (MM), or Acute Myeloid Leukemia (AML).
100 Clinical Results associated with CD1d x TCRDV2
100 Translational Medicine associated with CD1d x TCRDV2
0  Patents (Medical) associated with CD1d x TCRDV2