Shanghai Junshi Biosciences Co., Ltd.

Shanghai Junshi Biosciences Co., Ltd.

SHJBF
Shanghai Junshi Biosciences Co., Ltd.US flagOther OTC
3.35
USD
- -
- -
4.84BMarket Cap
2016 Y
2017 Y
2018 Y
2019 Y
2020 Y
2021 Y
2022 Y
2023 Y
2024 Y
2025 Y
TTM
Revenue per Share
- -
- -
- -
0.99
1.93
4.51
1.58
1.52
1.98
2.48
0.12
Basic EPS, GAAP
-0.17
-0.42
-1.19
-0.95
-2.02
-0.8
-2.6
-2.32
-1.3
-0.84
-1.08
Free Cash Flow per Basic Share
-0.51
-0.9
-1.77
-2.62
-2.54
-1.71
-2.36
-2.89
-2.17
-1.27
-0.82
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
0.01
Book Value per Share
0.72
0.77
-0.79
-1.54
1.06
1.02
-6.3
-8.18
-9.48
-10.07
-8.92
Tangible Book Value per Share
1.48
1.47
5.52
3.81
7.04
9.28
10.57
7.31
5.92
5.86
6.66
Basic Weighted Avg Shares
760
760
602
784
825
893
917
985
985
1,007
976
Sales/Revenue/Turnover
4
1
1
775
1,595
4,025
1,453
1,503
1,948
2,498
116
Operating Margin (%)
-3,947.56
-30,116.64
-72,593.79
-98.97
-104.61
-14.73
-186.88
-163.19
-66.73
-37.03
-863.84
Depreciation Expense
9
18
30
60
151
263
294
303
284
281
- -
Net Income, GAAP
-132
-321
-716
-744
-1,666
-719
-2,386
-2,282
-1,282
-841
-1,056
Effective Tax Rate (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Profit Margin (%)
-3,512.56
-27,948.08
-76,703.85
-95.98
-104.44
-17.85
-164.16
-151.85
-65.82
-33.66
-907.66
Working Capital
526
452
2,439
1,306
3,206
3,815
5,431
3,075
1,750
1,646
2,490
LT Debt
- -
- -
392
772
573
583
886
1,213
2,006
2,850
1,748
Total Equity
1,127
1,119
3,321
2,989
5,841
8,332
9,794
7,340
5,950
6,073
6,623
Return on Invested Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Common Equity (%)
- -
-56.55
- -
- -
- -
-80.59
- -
- -
- -
- -
- -

Capital Structure

FRC

in mil. unless spec.
Dec'23
Mar'24
Jun'24
ST Debt
575
1,238
822
LT Borrowings
1,196
1,659
1,738
LT Finance Leases
17
15
10
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
986
986
985
Market Capitalization
15,545
14,475
- -

Working Capital

FRC

in mil. unless spec.
Dec'23
Mar'24
Jun'24
Total Current Assets
5,550
6,194
4,821
Cash, Cash Equivalents & STI
3,778
4,559
3,311
Accounts Receivable, Net
480
492
450
Inventories
538
536
554
Total Current Liabilities
2,475
2,968
2,331
Payables & Accruals
- -
- -
- -
ST Debt
575
1,238
822
Deferred Revenue
- -
- -
- -

Growth Rates

FRC

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
- -
3.65%
2.07%
Free Cash Flow
- -
-3.73%
-39.88%
Net Income, GAAP
- -
18.52%
-34.43%
Sales/Revenue/Turnover
- -
29.95%
28.23%
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2023
255
415
-670
- -
1,503
2024
381
405
- -
- -
1,948
2025
- -
- -
- -
- -
2,498

Quarterly Earnings Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2023
-0.55
- -
- -
- -
-2.32
2024
-0.29
- -
- -
- -
-1.3
2025
- -
- -
- -
- -
-0.84

Quarterly Dividends Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2023
0.01
- -
- -
- -
- -
2024
0.01
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -

Company Description

APIChat
CEO
Cong Li
Full Time Employees
2,578
Sector
Healthcare
Industry
Biotechnology
Address
Building 7 Shanghai People's Republic of China 200126
IPO Date
Feb 2, 2021
Business
Shanghai Junshi Biosciences Co., Ltd. (HKEX: 1877; SSE: 688180; OTC: SHJBF) develops, manufactures and commercializes innovative biopharmaceuticals focused on oncology, autoimmune diseases, metabolic disorders, neurological conditions and infectious diseases; its core products include toripalimab (TUOYI, PD-1 inhibitor; LOQTORZI internationally) approved for multiple indications such as nasopharyngeal carcinoma, esophageal squamous cell carcinoma, melanoma, non-small cell lung cancer, small cell lung cancer and urothelial carcinoma; adalimumab biosimilar (JUNMAIKANG, UBP1211, TNF-α inhibitor) for autoimmune conditions including Crohn's disease; ongericimab (JUNSHIDA, JS002, PCSK9 inhibitor) for hypercholesterolemia and mixed dyslipidemia including statin-intolerant patients; deuremidevir hydrobromide (MINDEWEI, VV116, RdRp inhibitor) for COVID-19; etesevimab for SARS-CoV-2; along with pipeline candidates such as tifcemalimab (BTLA), JS005 (IL-17A) for plaque psoriasis, JS212 (EGFR/HER3 bispecific ADC), JS207 (PD-1 x VEGF bispecific), UBP1213 (BLyS), JS103 (uricase), JS401 (ANGPTL3 siRNA) and JS010 (CGRP). Founded in 2012 and headquartered in Shanghai, China, the company operates innovation centers in Shanghai, Suzhou and Maryland, US, with production bases in Suzhou Wujiang and Shanghai Lingang, targeting patients globally through partnerships and serving primarily oncologists, rheumatologists, cardiologists and infectious disease specialists in China and expanding internationally. Recent developments encompass strategic commercialization alliances including a January 2025 distribution and marketing partnership with LEO Pharma for toripalimab (LOQTORZI) in Europe, prior collaborations with Coherus BioSciences for the US and Canada, Dr. Reddy's Laboratories for 21 countries, Rxilient Biotech for Southeast Asia and Hikma for the Middle East and North Africa; regulatory milestones feature NMPA approvals for ongericimab's supplemental NDAs in 2025 for statin-intolerant patients, toripalimab's 12th indication for first-line melanoma, sNDA acceptance for HER2-expressing urothelial carcinoma and Phase 3 success for JS005 in plaque psoriasis; international approvals include toripalimab in Singapore, UAE, Kuwait, Pakistan, Canada, UK, Australia and European Commission for NPC and ESCC; pipeline advances such as IND approval for JS212 in March 2025 and robust H1 2025 revenue growth of 49% driven by toripalimab expansions and NRDL inclusion.

Company News

APIChat
  • Junshi Biosciences Announces Primary Endpoints Met in Final Analysis of Phase 3 Study for Perioperative Toripalimab plus Chemotherapy for Resectable Stage II-III NSCLC

  • Junshi Biosciences Presents Results from JS207 (PD-1/VEGF BsAb) Phase 2 Combo Studies and JS212 (EGFR/HER3 ADC) FIH Phase 1/2 Study at AACR 2026

  • Junshi Biosciences Announces 2025 Full Year Financial Results and Provides Corporate Updates

  • Junshi Biosciences Announces NMPA Acceptance of New Drug Applications for Toripalimab Injection (Subcutaneous) Across 12 Indications

  • Junshi Biosciences Announces Strategic Collaboration with Antengene to Evaluate Combination Therapy with JS207 (PD-1/VEGF BsAb) and ATG-037 (Oral CD73 Inhibitor)

  • Antengene Announces Clinical Collaboration with Junshi Biosciences to Explore the Synergistic Potential of ATG-037 (Oral CD73 Inhibitor) In Combination with JS207 (PD-1/VEGF BsAb)

  • Junshi Biosciences Announces Primary Endpoints Met in JS001sc's Phase 3 Study for the 1ST-line Treatment of NSQ-NSCLC

  • Junshi Biosciences Announces FDA's Approval of IND Application for Phase 2/3 Clinical Study of JS207 for the Neoadjuvant Treatment of NSCLC Patients

  • TREOS Bio Partners with Charité Berlin and Junshi Biosciences to Launch Pivotal Phase II Clinical Trial in Refractory MSS Colorectal Cancer

  • Junshi Biosciences Announces 2025 Interim Financial Results and Provides Corporate Updates