News
Mission
Deliver “medicines that matter” to improve patient health and contribute to enhanced quality of life. At ARTham Therapeutics, we will create value by developing innovative medicines that are disease modifying and improve patient health.
Value
ARTham Therapeutics Inc., is a clinical stage biopharmaceutical company that will deliver ‘medicines that matter’ for patients. Our goal is to create innovative medicines that are disease modifying and satisfy significant unmet medical need. To deliver on cost and time efficiency, ARTham will run a virtual R&D operating model that seeks innovation through the best academic and business partners.
Team
Team

Hiroshi Nagabukuro PhD

Akira Tanaka PhD

Kanako Kuniyeda PhD

Toshinori Higashi PhD
Board of Directors

Yasutomi Kato
PhD
KAKEN PHARMACEUTICAL CO., LTD.
General Manager,
R&D Planning &
Project Management Department

Motonori Miyakawa
PhD
KAKEN PHARMACEUTICAL CO., LTD.
General Manager,
Business Development Department

Tomohiro Takaya
PhD
Audit and Supervisory Board Member
KAKEN PHARMACEUTICAL CO., LTD.
General Manager,
Legal Affairs &
Intellectual Property Department
Advisors

Naoto Uemura MD,PhD

Matt Devalaraja
PhD
Senior Corporate Development Advisor
CEO, Nipuna Therapeutics

Yoichi Miyamae
DVM,PhD
Safety/toxicology
Shin Nippon Biomedical Laboratories, Ltd.
Director, Scientific Affairs Division

Xian Jing Yao
MD,PhD
Regulatory
Adjunct Professor, Oita University

Daniel Weiss
MD,CPI
Clinical Pharmacology
Unravel hidden value
and deliver drugs that
ultimately help patients
Science
ART-001
New Effective Treatment for Vascular Malformations
ART-001: First in Class PI3K (phosphatidylinositol-3-kinase) inhibitor for
the treatment of vascular malformations and overgrowth syndromes
- Significant unmet medical need with no current pharmacotherapy
- Patient with GOF mutation of PI3K-AKT pathway
- Selective inhibition of angiogenesis
- This program has received a grant from AMED, Japanese Agency for Medical Research and Development.
Vascular malformations are benign (non-cancerous) lesions that are present at birth,
but may become visible for weeks or months after birth. Unlike hemangiomas, vascular malformations
do not have a growth cycle and then regress but instead continue to grow slowly throughout life.
Most vascular malformations are sporadic (occurring by chance),
though some are inherited in a family as an autosomal dominant trait.
ART-648
Orally available phosphodiesterase type 4 (PDE4) inhibitor
- Broad spectrum anti-inflammatory effects via intracellular cAMP increase
- Preclinical validation of anti-fibrotic and anti-obesity effects
- Opportunities to treat dermal (bullous pemphigoid, psoriatic arthritis),
metabolic (NASH) and respiratory (COPD, IPF) disorders with high unmet medical needs - Optimal pharmacokinetic and safety/tolerability profile demonstrated in Phase 1 clinical study in healthy subjects
Indication: Bullous Pemphigoid
- A rare autoimmune chronic skin disorder resulting in generalized, pruritic, bullous lesions
- Autoantibodies recognize components of the basement membrane zone called BP180 and BP230
- Primarily a geriatric dermal disorder that occurs in patients aged >70 years
- Usually starts with redness and itching of the skin, and within weeks to months, thin-walled, tense blisters appear
over whole body - Mucous membranes may also be involved, but less common
- Topical and systemic corticosteroids as standard cares for patients with moderate-severe conditions
- Prevalence in the US: 12 /100,000 adults; 38/100,000 adults aged ≥60 years (Wertenteil et al., 2018)
- ~7,000 patients in Japan (Japan Intractable Diseases Information Center); ~20,000 patients including patients with mild symptoms
- R&D grant from the Japan Agency for Medical Research and Development (AMED) Program for Orphan Drugs prior
to Designation awarded since FY2020
