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A congenital disorder (due to inherited enzyme abnormality) or acquired (due to failure of a metabolically important organ) disorder resulting from an abnormal metabolic process.
Biomarker and diagnostic research for metabolic disease has been reported in the published literature.
146 clinical trials registered, 31 recruiting. Interventions under study include other interventions, medical devices, drug therapy, and procedural interventions. Pipeline includes 1 PHASE4, 3 PHASE3, 9 PHASE2. Research is primarily sponsored by academic and government institutions.
NCT ID | Title | Phase | Sponsor | Status |
|---|---|---|---|---|
[NCT06568471](https://clinicaltrials.gov/study/NCT06568471) |
Data assembled from 3 of 12 sources · Last updated Nov 2, 2026, 2:58 PM UTC
A Study on Efficacy and Safety of HST101 in Chinese Patients with Hypercholesterolemia |
PHASE3 |
Hasten Biopharmaceutical Co., Ltd. |
RECRUITING |
[NCT07343336](https://clinicaltrials.gov/study/NCT07343336) | Landscape of Gout in French Polynesia. | — | Lille Catholic University | RECRUITING |
[NCT01143454](https://clinicaltrials.gov/study/NCT01143454) | Characterization of Patients With Uncommon Presentations and/or Uncommon Diseases Associated With the Cardiovascular System | — | National Heart, Lung, and Blood Institute (NHLBI) | RECRUITING |
[NCT06092346](https://clinicaltrials.gov/study/NCT06092346) | A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders | — | National Human Genome Research Institute (NHGRI) | RECRUITING |
[NCT04644016](https://clinicaltrials.gov/study/NCT04644016) | Cord Blood Transplant in Children and Young Adults With Blood Cancers and Non-malignant Disorders | PHASE2 | Memorial Sloan Kettering Cancer Center | RECRUITING |
441 publications have been identified in PubMed for metabolic disease. Kisho has analyzed 309 by research type. Research spans Review / Meta-Analysis (54%), Basic Science / Preclinical (17%), and Other (11%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 168 | 54% |
Laboratory research | 54 | 17% |
Other research | 34 | 11% |
Disease patterns and progression | 27 | 9% |
Patient case studies | 9 | 3% |
New treatment approaches | 9 | 3% |
Clinical study results | 6 | 2% |
Testing and diagnosis research | 2 | 1% |
Liu Y (2026). [PMID: 40854106](https://pubmed.ncbi.nlm.nih.gov/40854106/). *FEBS Lett*. [Review / Meta-Analysis]
Bordelon CL (2026). [PMID: 41961206](https://pubmed.ncbi.nlm.nih.gov/41961206/). *Curr Diab Rep*. [Review / Meta-Analysis]
Zhang R (2026). [PMID: 41887981](https://pubmed.ncbi.nlm.nih.gov/41887981/). *Trends Endocrinol Metab*. [Review / Meta-Analysis]
Hamdan A (2026). [PMID: 42093245](https://pubmed.ncbi.nlm.nih.gov/42093245/). *Curr Opin Clin Nutr Metab Care*. [Review / Meta-Analysis]
Rosenmayr-Templeton L (2026). [PMID: 41837446](https://pubmed.ncbi.nlm.nih.gov/41837446/). *Ther Deliv*. [Review / Meta-Analysis]
Jia G (2026). [PMID: 41601324](https://pubmed.ncbi.nlm.nih.gov/41601324/). *Metabolism*. [Other]
Lian S (2026). [PMID: 42066736](https://pubmed.ncbi.nlm.nih.gov/42066736/). *J Nutr Health Aging*. [Other]
Ardisasmita AI (2026). [PMID: 41806328](https://pubmed.ncbi.nlm.nih.gov/41806328/). *J Inherit Metab Dis*. [Review / Meta-Analysis]
Zhou XD (2026). [PMID: 41854965](https://pubmed.ncbi.nlm.nih.gov/41854965/). *Sci China Life Sci*. [Review / Meta-Analysis]
Wolf E (2026). [PMID: 41291984](https://pubmed.ncbi.nlm.nih.gov/41291984/). *Reprod Fertil Dev*. [Review / Meta-Analysis]
AI-curated news mentioning metabolic disease
Updated Oct 14, 2026
Zealand Pharma has entered a deal worth up to $1.2 billion with Generate:Biomedicines to leverage its generative AI platform for developing new multispecific drug candidates targeting obesity and metabolic diseases. This partnership highlights the growing trend of integrating AI in drug discovery.
A pilot study in the Netherlands demonstrates the effectiveness of case-based telelearning in improving healthcare for patients with metabolic diseases. This innovative approach could enhance knowledge sharing among healthcare professionals managing rare diseases.
Roche has entered a partnership with Atavistik, potentially worth up to $2 billion, to develop new drugs targeting cardiometabolic diseases. This collaboration aligns with Roche's recent R&D expansion in Boston focused on cardiovascular, renal, and metabolic conditions.
Experts discuss how biopharma partnerships are evolving, as companies look beyond transactional supplier relationships toward more integrated, strategic, and collaborative models The best partnerships are not just financial transactions. They help determine whether a product can deliver meaningful clinical benefit, fit the realities of healthcare delivery, and create value that supports adoption. ... The most consequential shift is geographic. Chinese biotechs have become a primary source of licensed assets, particularly in ADCs and increasingly in others (e.g., metabolic disease, CNS, and autoimmune programs). BMS signed a strategic partnership worth $15.2 billion with Hengrui last month spanning 13 early-stage programmes across oncology, haematology, and immunology – the Company’s first major, modern-day, China-sourced innovation and licensing "blockbuster" deal. For European and US biotechs, this raises the competitive bar significantly. However, the quality of the early evidence package remains critical: robust non-clinical data, well-designed early clinical studies, clear differentiation, and a credible development strategy are what make later partnerships possible. In this sense, the market has shifted toward a model where small biotech companies are not just innovation sources, but key drivers of early value creation. As therapies become more complex, partnership models are evolving beyond the traditional customer-supplier relationship. Increasingly, companies are looking for partners who can contribute expertise, provide strategic input and help navigate challenges, rather than simply deliver against a predefined scope of work. Many emerging biotech companies operate with lean teams and rely on external partners to supplement their internal capabilities.
The Life Sciences industry, including pharmaceuticals, biotechnology, medical devices and diagnostics, has long relied on mergers and acquisitions (M&A) to drive innovation, expand portfolios and respond to evolving market demands. Big Pharma is acquiring biotech to fill pipeline gaps: Large pharma companies are facing major patent expirations and revenue pressure, so they are buying biotech assets to access new drugs, platforms and late-stage candidates. Oncology remains central, but interest is also rising in immunology, neuroscience, rare disease, metabolic disease, radiopharmaceuticals and cell therapies. For example, Brickell’s deal with Botanix used milestone and sales-based earnouts, and Bristol-Myers Squibb’s acquisition of Celgene used a CVR tied to future regulatory milestones. Overall, risk-sharing remains central to these transactions, with parties allocating uncertainty through contingent payments, milestone triggers, profit-sharing, financing support, regulatory covenants, termination protections and post-closing carve-out obligations. The pharma and biotech M&A landscape is being shaped by the need for innovation, portfolio renewal and access to advanced technologies. Cross-border deals are increasing: Pharma companies are sourcing more innovation globally, especially from China, Japan and Europe. China has become a major source of biotech innovation, but geopolitical and regulatory risks are pushing companies toward licensing, co-development, option deals and milestone-based structures rather than full acquisitions alone. Cross-border and alternative structures will increase: Innovation will remain globally distributed, with continued interest in China, Japan, Europe and emerging biotech hubs. Because geopolitical, IP, data and supply-chain risk can complicate outright acquisitions, more companies are likely to use licensing, regional rights, joint development, options, royalties, minority investments and CVRs to access innovation while managing risk.