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TGA / PMDA / NMPA · Asia-Pacific

teplizumab — TGA / PMDA / NMPA regulatory status

teplizumab (TEIZEILD) regulatory status in the Asia-Pacific is tracked from public TGA / PMDA / NMPA records and cross-linked clinical and patent datasets on NovaPharmaNews. Current status: NMPA clinical trials.

Status snapshot

Status
NMPA clinical trials
Brand
TEIZEILD
Mechanism
T-cell surface glycoprotein CD3 epsilon chain other
Target
T-cell surface glycoprotein CD3 epsilon chain
Structured fields
6

Pharmacology context used for competitive intelligence: T-cell surface glycoprotein CD3 epsilon chain other. Target: T-cell surface glycoprotein CD3 epsilon chain. This page is a status aggregation for professional reference — not prescribing advice.

Regional decision snapshot — NMPA: clinical trials.

Linked evidence on this spoke: 2 published clinical programs and 0 related patent records. Use the tables below for NCT identifiers, phases, and exclusivity dates; verify against primary sources before BD or medical decisions.

Regulatory timeline

Regulator Region Status Date Source
NMPA China clinical trials Evidence

Linked clinical programs

Program Phase Sponsor NCT
Teplizumab Phase 3 Sanofi Pasteur MSD NCT07088068
Teplizumab, Matched placebo for test product Phase 3 Sanofi-Aventis U.S 2024-519494-19-00

Related hubs

FAQ

What is the TGA / PMDA / NMPA approval status of teplizumab?

teplizumab currently shows NMPA clinical trials in our Asia-Pacific regulatory index. Confirm on the official TGA / PMDA / NMPA label or EPAR before clinical or commercial use.

Where does NovaPharmaNews get teplizumab regulatory data?

Status fields are joined from public sources (openFDA / EMA / regional agencies), ClinicalTrials.gov-linked programs, and patent registries. See /about/data-sources for attribution.

How many clinical programs are linked to teplizumab?

This spoke lists 2 published programs associated with teplizumab in our pipeline index.