Tobevibart

Drug

Drug Profile

Tobevibart (VIR-3434) is an investigational broadly neutralizing monoclonal antibody in clinical development for chronic hepatitis delta, typically studied in combination with elebsiran. Phase 2 data reported high rates of undetectable HDV RNA and the registrational ECLIPSE program is ongoing with topline data expected in 2027. It is not approved for marketing.

Drug Class
Investigational broadly neutralizing monoclonal antibody targeting HBsAg
Approval Status
Investigational (registrational Phase 3 program underway; no U.S. approval)
Mechanism of Action
Targets HBsAg to inhibit HBV/HDV entry into hepatocytes, reduce circulating viral/subviral particles, and enhance immune-complex clearance via engineered Fc domain.
Indications
  • \Chronic hepatitis delta (investigational, typically in combination with elebsiran)\

Related News

Related Clinical Trials

NCT ID Title Status Phase
NCT07142811

A Study to Evaluate Tobevibart+Elebsiran Versus Bulevirtide in Chronic HDV Infection

ACTIVE_NOT_RECRUITING PHASE2
NCT07128550

A Study to Evaluate Tobevibart+Elebsiran in Participants With Chronic HDV Infection Not Virologically Suppressed With Bulevirtide

RECRUITING PHASE3
NCT06903338

A Study to Evaluate Tobevibart + Elebsiran in Chronic HDV Infection

ACTIVE_NOT_RECRUITING PHASE3