A MULTICENTER, FIRST-IN-HUMAN, DOSE ESCALATION AND OPTIMIZATION PHASE I/IIA STUDY TO INVESTIGATE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND EFFICACY OF THE NAPI2B ANTIBODY-DRUG CONJUGATE TUB-040 IN PATIENTS WITH PLATINUM-RESISTANT HIGH-GRADE OVARIAN CANCER (PROC) OR RELAPSED/REFRACTORY ADENOCARCINOMA NON-SMALL CELL LUNG CANCER (NSCLC) (NAPISTAR 1-01).

Registry ID
NAPISTAR 1-01
Source registry
HEALTH_CANADA
Status
Pending
Phase
PHASE1
Study type
INTERVENTIONAL
Sponsor
TUBULIS GMBH
Last update
2026-05-22

Conditions

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