focuses on the research and development of differentiated products in four major therapeutic areas: oncology, anti-infection, gastrointestinal, and central nervous system. (Disclosed projects only)

4

PCC

1

IND

2

Clinical

2

Launched

9

Total

Oncology

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Projects:

DN022150

Target:

KRAS G12D

Indications:

Solid tumor

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Anti-Infection

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Projects:

GP681(Suraxavir Marboxil Tables)

Target:

PA

Indications:

influenza

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

On March 27, 2025, Suraxavir Marboxil Tablets (brand name: Yisuda) received marketing approval from the National Medical Products Administration (NMPA). It is indicated for the treatment of uncomplicated influenza A and B in previously healthy adolescents and adults aged 12 and older.

Phase III clinical trial data were published in the prestigious global medical research journal Nature Medicine.

Single-dose suraxavir marboxil for acute uncomplicated influenza in adults and adolescents: a multicenter, randomized, double-blind, placebo-controlled phase 3 trial.

Nature Medicine, 2025 Jan 7.
doi: 10.1038/s41591-024-03419-3

ClinicalTrials.gov registration: NCT05474755.

Projects:

GP681(Dry Suspension)

Target:

PA

Indications:

influenza

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Projects:

KR24258

Target:

-

Indications:

-

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Gastrointestinal System

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Projects:

Aurantii Fructus Immaturus Total Flavonoids Tablet

Target:

-

Indications:

Gastrointestinal motility

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Aurantii Fructus Immaturus Total Flavonoids Tablet (Brand name: Orante) is an innovative Class 1.2 traditional Chinese medicine developed by Qingfeng Pharmaceutical. The main ingredient is total flavonoid extract of Aurantii Fructus Immaturus, used for functional dyspepsia.

The two Phase III clinical trials (placebo-controlled and compared with Domperidone) show that Aurantii Fructus Immaturus Total Flavonoids Tablet have good therapeutic effects on common symptoms of functional dyspepsia (such as liver-stomach disharmony, spleen-stomach damp-heat, food stagnation, and spleen-stomach deficiency). The trials also showed that symptom relief persisted after discontinuation, with a better safety profile and sustained efficacy than the active comparator drug.

Central Nervous System

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Projects:

KR232

Target:

-

Indications:

-

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched


Projects:

KR233

Target:

-

Indications:

-

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Projects:

KR25102

Target:

-

Indications:

-

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Others

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

Projects:

KR230109

Target:

-

Indications:

-

Projects

Target

Indications

PCC

IND

Phase I/II

Phase III

NDA

Launched

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