RaQualia Pharma Inc.

Tokyo Stock Exchange:4579.T

Location

Market Cap

USD 90.99 M

Share Price

USD 3.75

Avg Daily Volume

298,219

Change (1 day)

-2.37%

Change (1 year)

-6.49%

Change (YTD)

53.08%

RaQualia Pharma Inc. Shareholders' Equity for the year ending December 31, 2024: USD 35.43 M

RaQualia Pharma Inc. Shareholders' Equity is USD 35.43 M for the year ending December 31, 2024, a -18.32% change year over year. Shareholders' equity are the residual interest in the assets of a company after deducting liabilities, representing the shareholders' ownership claim.
  • RaQualia Pharma Inc. Shareholders' Equity for the year ending December 31, 2023 was USD 43.38 M, a 3.50% change year over year.
  • RaQualia Pharma Inc. Shareholders' Equity for the year ending December 31, 2022 was USD 41.91 M, a 0.77% change year over year.
  • RaQualia Pharma Inc. Shareholders' Equity for the year ending December 31, 2021 was USD 41.59 M, a 7.14% change year over year.
  • RaQualia Pharma Inc. Shareholders' Equity for the year ending December 31, 2020 was USD 38.82 M, a -8.69% change year over year.
Key data
Date Shareholders' Equity Cash and Short-Term Investments Receivables Inventory
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Tokyo Stock Exchange: 4579.T

RaQualia Pharma Inc.

CEO Masaki Sudo
IPO Date July 20, 2011
Location Japan
Headquarters Meieki Southside Square
Employees 64
Sector 🏥 Health Care
Industries
Description

RaQualia Pharma Inc. engages in the research and development of pharmaceutical compounds worldwide. Its human products portfolio includes tegoprazan for gastroesophageal reflux disease, which is in phase 1 clinical trial in the United States; and grapiprant for pain management, which is in phase II clinical trial in the United States and phase I clinical trial in China, as well as in phase I clinical trial in China and the United States to treat cancer. The company also provides veterinary products such as, grapiprant for osteoarthritis in dogs; ghrelin receptor agonist to treat cancer-related anorexia/cachexia syndrome, and constipation resulting from spinal cord injury; and ELURA, a drug for the management of weight loss in cats with chronic kidney disease. In addition, it provides TRPM8 blocker for the target indication of neuropathic pain; motilin receptor agonist to treat gastrointestinal dysmotility, including gastroparesis, functional dyspepsia, and post-operative ileus; potassium-competitive acid blocker to treat gastro-esophageal reflux disease that has completed phase 1 clinical trial; 5-HT4 partial agonist to treat gastroparesis, functional dyspepsia, and chronic constipation; 5-HT2B antagonist to treat irritable bowel syndrome with diarrhea; EP4 antagonist, a pain management drugs for dogs; serotonin 5-HT2A and dopamine D2 receptor blocker to treat schizophrenia; EP4 antagonist to treat cancer that is in phase I clinical trial, as well as in phase 1 clinical trial for the indication of pain; Cyclooxygenase-2 inhibitor, Phase I clinical trials for the indication of pain; CB2 agonist; selective sodium channel blocker; P2X7 receptor antagonist, which is in Phase I clinical trials for the target indication of neuropathic pain; and retinoic acid receptor alpha agonist. It has a collaborative agreement with Interprotein Corporation, ASKA Pharmaceutical. Co., Ltd., and Epigeneron, Inc. The company was incorporated in 2008 and is headquartered in Nagoya, Japan.

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