Partnering

Ryusuke Sakamoto
General Manager, Business Development Department

Sanwa Kagaku Kenkyusho is a valued member of the Suzuken Group, specializing in pharmaceuticals and diagnostics. Through our business development activities, we are committed to realizing our vision: "Patient-friendly 'medicines' for people around the world."
Also, We have been addressing the issue of 'drug loss' in Japan-where drugs approved in the U.S. and/or Europe are not available in Japan- We have introduced the "J-Entry Consortium", a new market entry option. Our strength lies not only in offering traditional licensing structures but also in providing diverse partnership opportunities tailored to different needs. Let's discuss how we can collaborate!

Our Partnering Strategy

Discovery→Optimization Research→Preclinical→Early clinical Phase 1-2a→Late Clinical Phase 2b-3→marketing

Our In-licensing Focus

Asset Strategy

Therapeutic Areas

Endocrine,
metabolic disorders
Neurological disorders
Rare diseases

Modalities(Small molecule,Peptide,Protein,Nucleic acid)

Small molecule

Peptide

Protein

Nucleic acid

Development Status

1st Priority Phase 2 ~ Phase 3
(With data on efficacy andsafety in clinical trials for the target indications)
2nd Priority GLP ~ Phase 1
3rd Priority Phase 2 ~ Phase 3
(Without data on efficacy and safety in clinical trials for the target indications)

Assets that are considered to have clear clinical positioning and competitive advantages

J-ENTRY Consortium

J-ENTRY Consortium

We offer a unique solution-the J-ENTRY Consortium (JEC)-to facilitate entry into the Japanese market. In collaboration with Suzuken (Distributor), EPS Group (CRO), and Bushu Pharma (CDMO), we are committed to addressing the issue of 'drug loss.'
JEC provides a comprehensive, one-stop service for entering the Japanese market, covering the entire process from drug development and J-NDA submission for marketing authorization (MA) to sales, marketing, and distribution.

One-stop solution by a three-company collaboration

Designated Marketing Authorization Holder(DMAH)↔Licensor[Development Phase→J-NDA〜MA→Commercialization]Providing all capabilities under your Strategy
Development Phase J-NDA〜MA Commercialization
  • Market research
  • Clinical trials
  • Regulatory affairs
  • Preparation of application documents
  • Application for approval
  • Regulatory affairs
  • NHI price negotiations
  • Post-marketing clinical trials, post-marketing surveillance
  • Sales & marketing
  • Medical Science Liaison
  • Clinical trials
  • Regulatory affairs
  • Preparation of application documents
  • Contact center
  • Manufacturing, testing and secondary packaging of clinical trial drugs
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  • Manufacturing, testing and secondary packaging of commercial products
- -
  • Manufacturer distribution
  • Wholesale business
  • Inventory control

Contact Us

We always welcome proposals for joint research and drug discovery collaborations.
Please feel free to contact us using the form below.

contact us

Details of alliance with the partner

Crinetics Pharmaceuticals

In February 2022, we entered into an exclusive licensing agreement with Crinetics Pharmaceuticals, Inc. for the development and commercialization of paltusotine in Japan. Paltusotine is Crinetics' investigational, orally available, once-daily, non-peptide somatostatin receptor type 2 (SST2) agonist, being evaluated as a treatment for acromegaly and carcinoid syndrome in neuroendocrine tumors.
We are currently conducting a local Phase 3 trial for acromegaly in Japan, while Crinetics has successfully completed two global Phase 3 trials for acromegaly and submitted a New Drug Application (NDA) in the United States in September 2024.

EA Pharma Co., Ltd.

In March 2014, we entered into an exclusive licensing agreement with Ajinomoto Pharmaceuticals Co., Ltd. (now EA Pharma Co., Ltd.) for the development and commercialization rights of Upacicalcet in Japan for secondary hyperparathyroidism (SHPT) in patients undergoing hemodialysis. At the time, the asset was in the non-clinical stage.
We successfully advanced all aspects of development, including CMC, non-clinical, and clinical studies, leading to marketing approval from the Ministry of Health, Labour and Welfare (MHLW) in August 2021.
Since then, we have been commercializing the product under the name Upasita® Injection Syringe for Dialysis in Japan, contributing to improved treatment for dialysis patients suffering from SHPT.

Nissan Chemical Industries, Ltd.

Sanwa Kagaku Kenkyusho and Nissan Chemical have successfully discovered a preclinical antisense candidate under the discovery collaboration agreement established in March 2019. Building on this achievement, our team and Nissan Chemical have decided to expand their strategic collaboration to develop additional oligonucleotide therapeutic programs.
Under this new collaboration, our team and Nissan Chemical are jointly conducting drug discovery research to identify novel oligonucleotide therapeutics. Nissan Chemical is responsible for designing and synthesizing oligonucleotide molecules targeting areas selected by both parties, while we oversee efficacy and toxicity studies.

Partnering

We have engaged in partnership agreements with numerous companies both domestically and internationally.

Our Pharmaceutical Business Partners

Bushu Pharmaceuticals
Crinetics Pharmaceuticals, Inc.
DAIICHI SANKYO ESPHA CO., LTD.
Dong-A ST Co., Ltd.
EA Pharma Co., Ltd.
EPS Corporation
FUJIFILM Toyama Chemical Co., Ltd.
FUJIYAKUHIN Co., Ltd.
HISAMITSU PHARMACEUTICAL CO.,INC.
JW Pharmaceutical Corporation
Kidswell Bio Corporation
Kissei Pharmaceutical Co., Ltd.
KOLON PHARMA Co., Ltd.
Methapharm Inc.
Nissan Chemical Co.,
Samjin Pharmaceutical Co., Ltd.

Our Diagnostic Business Partners

Abbott Japan LLC
ADVANTEC TOYO KAISHA, LTD.
ARKRAY, Inc.
Asahi Polyslider
Minaris Medical
PHC Corporation
Roche Diagnostics
SAKAE Co., Ltd.

OSDrC® Business Partners

Novartis
TAIHO PHARMACEUTICAL CO., LTD.

Our Other Business Partners

Elanco Animal Health

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