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TGA / PMDA / NMPA · Asia-Pacific

erythropoietin — TGA / PMDA / NMPA regulatory status

erythropoietin 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
Structured fields
4

Regional decision snapshot — NMPA: clinical trials.

Linked evidence on this spoke: 12 published clinical programs and 5 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

Related patents

Number Title Jurisdiction
11197812 Cosmetic formulations for topical applications containing erythropoietin-derived molecules US
10912791 Compositions comprising antisense-encoded erythropoietin receptor and use thereof US
10456346 Cosmetic formulations for topical applications containing erythropoietin-derived molecules US
10233452 Compositions and methods for increasing erythropoietin (EPO) production US
7300915 Use of erythropoietin and erythropoietin mimetics for the treatment of neuropathic pain US

Related hubs

FAQ

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

erythropoietin 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 erythropoietin 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 erythropoietin?

This spoke lists 12 published programs associated with erythropoietin in our pipeline index.