Focusing on innovation and patient accessibility, we have established a diversified and complementary R&D pipeline. Most products are independently developed through our own platform, and we have a number of potential novel antitumor targets drugs. Our products respond to a vast array of diseases, including cancer, autoimmune, metabolic, neurological, and infectious diseases.
As we continue to enrich our pipeline and explore combination treatments, our fields of innovation R&D has expanded from monoclonal antibodies to small molecule drugs, polypeptide drugs, antibody-drug conjugates (ADCs), bispecific antibody or multispecific antibody drugs, nucleotide drugs and etc. We will continue to further explore the next generation of innovative therapies for cancer and autoimmune diseases.
PD-1+VEGF
Tumors
A recombinant humanized anti-PD-1/VEGF bispecific antibody self-developed by the company
CD3+CD20
Tumors
PD-1+TGF-β
Tumors
HDACs
Tumors
KRAS
Tumors
EGFR 4th Gen
NSCLC
Aurora A
SCLC
EGFR exon 20
NSCLC
XPO1
Endometrial cancer
A small molecule inhibitor of the nuclear export protein XPO1
TROP2 ADC
TNBC
Claudin18.2 ADC
Gastrointestinal cancer
An antibody-drug conjugate (ADCs) targeting Claudin18.2 developed by Junshi Biosciences
PI3K-α
Gynecological tumors
An oral small molecule inhibitor targeting PI3K-α jointly developed by Junshi Biosciences and Risen Biosciences
Pan-CDK
Breast cancer, etc.
CD39
Tumors
A recombinant fully human anti-CD39 monoclonal antibody developed by Suzhou Kebo Ruijun owned by Junshi Biosciences and Beijing Enruini
DKK1
Tumors
A recombinant humanized anti-DKK1 monoclonal antibody developed independently by the company
IL-21
Tumors
A fusion protein consisting of recombinant IL-21 and nanobody against human serum albumin (HSA) co-developed by Junshi Biosciences and Anwita Biosciences
Claudin 18.2
Gastric cancer
CD112R/PVRIG
Tumors
A recombinant humanized monoclonal antibody against human CD112R developed independently by Junshi Biosciences
CTLA-4
Lung cancer, melanoma
A recombinant humanized anti-CTLA-4 monoclonal antibody developed independently by Junshi Biosciences
TIGIT
Tumors
A recombinant humanized anti-TIGIT monoclonal antibody developed independently by Junshi Biosciences
PD-L1
Tumors
S protein
COVID-19
BLyS
Systemic lupus erythematosus
Small nucleic acid immunomodulator
Seasonal allergic rhinitis
A small nucleic acid immunomodulator jointly developed by Junshi Biosciences and its partner JSIAMA Biopharmaceutical
ANGPTL3 (siRNA)
Metabolic diseases
JS401 is a siRNA drug targeting ANGPTL3 mRNA jointly developed by Junshi Biosciences and its partner Risen Medical
Uricase
Hyperuricacidemia
CGRP
Migraine
VEGF
NSCLC
BTLA
Lung cancer, lymphoma, etc
World’s first-in-human anti-BTLA mAb against tumor
IL-17A
Psoriatic, spondylitis
An anti-IL-17A monoclonal antibody developed independently by Junshi Biosciences
PD-1
Tumors
A subcutaneous injection formulation developed by Junshi Biosciences on the basis of toripalimab
PD-1
Tumors
TNF-α
Rheumatoid Arthritis, etc
RdRp
COVID-19
VV116 is an oral nucleoside analog drug that can inhibit the replication of SARS-CoV-2
S protein
COVID-19
PCSK9
Hyperlipidemia
Ongericimab is a recombinant humanized anti-PCSK9 monoclonal antibody independently developed by Junshi Biosciences for the treatment of primary hypercholesterolemia and mixed dyslipidemia
Toripalimab is an anti-PD-1 monoclonal antibody developed for its ability to block PD-1 interactions with its ligands, PD-L1 and PD-L2, and for enhanced receptor internalization (endocytosis function). Blocking PD-1 interactions with PD-L1 and PD-L2 promotes the immune system’s ability to attack and kill tumor cells.
More than forty company-sponsored toripalimab clinical studies covering more than fifteen indications have been conducted globally by Junshi Biosciences, including in China, the United States, Southeast Asia, and Europe. Ongoing or completed pivotal clinical trials evaluating the safety and efficacy of toripalimab cover a broad range of tumor types, including cancers of the lung, nasopharynx, esophagus, stomach, bladder, breast, liver, kidney, and skin.
In the Chinese mainland, toripalimab was the first domestic anti-PD-1 monoclonal antibody approved for marketing (approved in China as TUOYI®). Currently, there are ten approved indications for toripalimab in the Chinese mainland:
All of the 10 indications have been included in the National Reimbursement Drug List (NRDL) (2024 Edition). Toripalimab is the only anti-PD-1 monoclonal antibody included in the NRDL for the treatment of melanoma, renal carcinoma and TNBC, and perioperative treatment of NSCLC. In October 2024, toripalimab for the treatment of recurrent or metastatic NPC was approved in Hong Kong SAR, China.
In terms of international layout, toripalimab has been approved for marketing in the United States, the European Union, India, the UK, Jordan and other countries and regions. In addition, the Australia Therapeutic Goods Administration (TGA) and the Singapore Health Sciences Authority (HSA) accepted the new chemical entity application and the new drug application for toripalimab in combination with cisplatin and gemcitabine, for the first-line treatment of adults with metastatic or recurrent locally advanced NPC, and for toripalimab, as a single agent, for the treatment of adults with recurrent, unresectable, or metastatic NPC with disease progression on or after platinum-containing chemotherapy, respectively.
PD-1 is a T cell surface receptor; it is an immune checkpoint molecule in the co-inhibitory signal pathway of the T cell. As shown in the following figure, the binding of the PD-1 ligands, PD-L1 and PD-L2, to the PD-1 receptor found on T cells inhibits T cell proliferation and cytokine production. Upregulation of PD-1 ligands occurs in some tumors and signaling through this pathway can contribute to the inhibition of T-cell activation and immune surveillance of tumor cells. Anti-PD-1 monoclonal antibodies can block the PD-1/PD-L1 pathway and thereby restore the immune function of T cells.