Main Programs (Human)

Potassium-Competitive Acid Blocker(P-CAB)K-CAB®tegoprazan / RQ-00000004

Target Indication: Gastroesophageal Reflux Disease

Under Review: Vietnam, etc.

Partnered Party: HK inno.N Corporation

Licensed Territory: Worldwide Excluding Japan

※区切り線が入ります。

Phase 3 Ongoing: U.S.

Partnered Party: HK inno.N Corporation

Licensed Territory: Worldwide Excluding Japan

※区切り線が入ります。

Phase 1 Completed: Japan

Partnering Activity Underway

Licensed Territory: Japan

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Potassium-Competitive Acid Blocker(P-CAB) Overview

Tegoprazan is a novel Potassium-Competitive Acid Blocker (P-CAB), a new type of gastric acid secretion inhibitor. Proton pump inhibitors (PPIs) have been used from long ago for gastroesophageal reflux disease, however, P-CAB as a new generation of drugs suppresses gastric acid secretion more rapidly and more persistently than PPIs.

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Ghrelin Receptor AgonistRQ-00433412

Target Indication: Constipation, Cancer-Related Anorexia/ Cachexia Syndrome

Pre-Clinical Studies Ongoing

Partnering Activity in Preparation

Licensed Territory: Worldwide

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Ghrelin Receptor Agonist Overview

RQ-00433412 is a novel ghrelin receptor agonist discovered by RaQualia. Ghrelin receptors regulate feeding and growth hormone secretion. Ghrelin receptor agonists are known to improve cachexia, weight loss, and anorexia in cancer patients. In addition to these effects, RQ-00433412 is expected to be an innovative new therapeutic option that improves quality of life of patients with constipation by promoting spontaneous bowel movement without causing diarrhea based on its gastrointestinal prokinetic effect.

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Sodium Channel BlockerRQ-00350215

Target Indication: Pain

Undisclosed

Partnered Party: Hisamitsu Pharmaceutical Co., Inc.

Licensed Territory: Worldwide

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Sodium Channel Blocker Overview

RQ-00350215 is a novel sodium channel blocker discovered by RaQualia. Sodium channels, together with other ion channels such as potassium channels, control the generation and transmission of nerve action potentials and thus are deeply involved in neurotransmission. By selectively blocking the function of specific sodium channels involved in the transmission of pain signals, RQ-00350215 is expected to be an epoch-making new drug for chronic pain for which existing drugs do not provide sufficient analgesic effect.

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TRPM8 BlockerRQ-00434739 / XG2002

Target Indication: Chronic Pain

Phase 1 Ongoing: Australia

Partnered Party: Xgene Pharmaceutical Co. Ltd.

Licensed Territory: Worldwide excluding Japan

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TRPM8 Blocker Overview

RQ-00434739 is a novel Transient Receptor Potential Melastatin 8 (TRPM8) blocker discovered by RaQualia. TRPM8 is a temperature-sensitive ion channel that is activated by cold stimuli below 28 ℃ or menthol (a component of mint), and has been suggested to play roles in various pathological conditions including pain. RQ-00434739 has shown efficacy in animal models of pain through a new mechanism of action different from those of existing drugs, and is expected to be a breakthrough new drug for chronic pain for which treatment satisfaction is still low.

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