Monday, July 13, 2026

TGA / PMDA / NMPA · Asia-Pacific

intravenous — TGA / PMDA / NMPA regulatory status

intravenous 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: 129 published clinical programs and 12 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
1001 Phase 3 Biotest Farmaceutica Ltda 2024-513002-60-00
160701 Phase 3 Takeda NCT00818662
161003 Phase 3 Takeda NCT01524887
161202 Phase 3 Takeda NCT01736579
170904 Phase 3 Takeda NCT01218438
61186372NSC3001 Phase 3 Janssen-Cilag International N.V 2023-506033-29-00
61186372NSC3002 Phase 3 Janssen-Cilag International N.V 2023-506518-33-00
8951-CL-0301 Phase 3 Astellas Pharma 2024-511365-11-00
8951-CL-0302 Phase 3 Astellas Pharma 2024-511648-16-00
8951-CL-0305 Phase 3 Astellas Pharma 2024-519773-19-00
ALN-TTR02-011 Phase 3 Alnylam Netherlands 2023-508364-29-00
AV-299-23-301 Phase 3 Anaxis Pharma 2023-505606-42-00

Related patents

Number Title Jurisdiction
12371333 Purification of clinoptilolite US
12343350 Istaroxime-containing intravenous formulation for the treatment of acute heart failure (AHF) US
2025002606 Combination Therapy for Treating Cancer with an Antibody and Intravenous Administration of a Recombinant MVA US
2023302008 METHODS OF ADMINISTERING INTRAVENOUS MELOXICAM IN A BOLUS DOSE US
11629060 Purification of clinoptilolite US
11596610 Compositions in support of health and mental accuity US
11583540 Istaroxime-containing intravenous formulation for the treatment of acute heart failure (AHF) US
11197869 Istaroxime-containing intravenous formulation for the treatment of acute heart failure (AHF) US
11202104918P THERAPY FOR TREATING CANCER WITH AN INTRATUMORAL AND/OR INTRAVENOUS ADMINISTRATION OF A RECOMBINANT MVA ENCODING 4-1BBL (CD137L) AND/OR CD40L SG
10117937 Highly branched alpha-D-glucans US
10010534 Intravenous formulation and LC/MS/MS analysis method for GMC1 US
9675572 Intravenous omega-3 fatty acid compositions and method of use US

Related hubs

FAQ

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

intravenous 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 intravenous 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 intravenous?

This spoke lists 129 published programs associated with intravenous in our pipeline index.