Market atlas / Alpha-glucosidase / Acarbose
Acarbose (ITP-validated geroprotector)
repurposedsmall-moleculealpha-glucosidase-inhibitionpostprandial-glucosegut-microbiome● postprandial-glucose
Stage by geography
United Kingdom leads by 4 stages. Singapore reached it about 30 years before Israel.
signalpreclinfirst-in-humanRCTapprovedreal-worldconsumerUSUKCNSGILKRINJP+4 stages
MarketsUS United States FDAUK United Kingdom MHRA / NICECN China NMPAIN India CDSCOJP Japan PMDACH Switzerland SwissmedicSG Singapore HSAIL Israel Ministry of HealthKR South Korea MFDS
What each market approved it for
| Market | Stage | Since | Indication / class / form |
|---|---|---|---|
| US | approved | not dated | class alpha-Glucosidase Inhibitor [EPC] |
| UK | approved | 2018-12-14 | indication Indications Acarbose is recommended for the treatment of non-insulin dependent (NINNM) diabetes mellitus in patients inadequately controlled on diet alone, or… |
| CN | approved | not dated | form Tablet, chemical drug |
| IN | signal | 2008-04-01 | not published |
| JP | RCT | not dated | not published |
| SG | approved | 1994-10-01 | form Tablet, oral, prescription only |
| IL | approved | 2025-01-31 | indication Treatment of non-insulin dependent diabetes mellitus (NIDDM) in patients inadequately controlled on diet alone, or on diet and oral hypoglycaemic agents. |
| KR | approved | 1999-12-23 | class Diabetes agents [MFDS 03960] |
China registers · NMPA
What each NMPA register actually approved. Reference approval NMPA H20244564. Domestic generics vs imported originator.
34domestic approvals
- Forms listed
- 4
- Product
- Acarbose Tablets
- Form
- tablet
- Strength
- 100mg
- Holder
- Zhejiang Jingxin Pharmaceutical
- Origin
- China
- Approved
- 2024-07-30
- Approval no
- NMPA H20244564
1imported approvals
approval count only; per-product detail not captured
Biomarker trends
no biomarker readings yet
Studies
The studies on Acarbose, what they found, in whom and how strongly, are on its evidence page, each linked to its source.
What the trials measure
Registered primary outcomes this development's trials are powered on, commonest first (ClinicalTrials.gov). What is measured, across markets.
| Registered primary endpoint | Markets measuring it |
|---|---|
| Data collection on patients weight and waist circumference, fasting blood glucose, postprandial blood glucose (2h), HbA1C… | IN, KR, SG |
| Change in fasting blood glucose levels | IN |
| Change in post-prandial glucose values | IN |
| Change in Hemoglobin A1c (HbA1c) levels | IN |
| Data collection on body weight | IN |
| Data collection on blood glucose | IN |
| Data collection on Hba1c | IN |
| Data collection on pre treatment concomitant diseases | IN |
| Mean change in HbA1c | IN |
| Incidence of adverse drug reactions (ADRs) and serious adverse events (SAEs) | JP |
Connections
Trajectory
1994
MarketSG: approved-other (HSA-registered (Singapore))
HSA:acarbose (1994-10-01) · machine-extracted
1999
MarketKR: approved-other (MFDS-approved (South Korea))
MFDS:acarbose (1999-12-23) · machine-extracted
2018
MarketUK: approved-other (MHRA-authorised (UK), per eMC SmPC)
EMC:acarbose (product 10000) · machine-extracted
2025
MarketIL: approved-other (Israel MoH-registered)
IsraelMoH:acarbose (2025-01-31) · machine-extracted
2026
MarketCN: approved-other (NMPA-approved (domestic + imported))
NMPA:NMPA H20244564 · machine-extracted
Get into the weeds: raw observations + provenance
hsa__dev_acarbose__SG 2026-07-13 kind=geography_stage verify=M HSA-registered in Singapore: ACARBOSE (GLUCOBAY 50 TABLET 50 mg), first registration 1994-10-01. [HSA Listing of Registered Therapeutic Products] source HSA:acarbose (1994-10-01) https://data.gov.sg/datasets/d_767279312753558cbf19d48344577084/view mfds__dev_acarbose__KR 2026-07-13 kind=geography_stage verify=M MFDS-approved in South Korea: Acarbose (Glucobay Tab. 100mg), first approval 1999-12-23. [MFDS drug product-approval list] source MFDS:acarbose (1999-12-23) https://nedrug.mfds.go.kr/pbp/CCBGA01 acar_in 2026-06-29 kind=geography_stage verify=M Acarbose: registered early-phase trials in India [NCT01613105] source NCT01613105 https://clinicaltrials.gov/study/NCT01613105 acar_edge_metf 2026-06-29 kind=edge verify=M both metabolic geroprotectors, carbohydrate-absorption vs AMPK source Harrison2014 https://doi.org/10.1111/acel.12170 acar_facets 2026-06-29 kind=facets verify=M Acarbose facets source Harrison2014 https://doi.org/10.1111/acel.12170 acar_uk 2026-07-14 kind=geography_stage verify=M UK marketing authorisation (MHRA), per the eMC SmPC: Acarbose 100 mg Tablets [active substance: acarbose], first authorised 2018-12-14. [electronic Medicines Compendium, medicines.org.uk] source EMC:acarbose (product 10000) https://www.medicines.org.uk/emc/product/10000/smpc israelmoh__dev_acarbose__IL 2026-07-13 kind=geography_stage verify=M Registered in Israel (Israeli Drug Registry): ACARBOSE 100 MG (ACROSE 100), current registration 2025-01-31. [Israel MoH Drug Registry] source IsraelMoH:acarbose (2025-01-31) https://israeldrugs.health.gov.il/ ctsearch__JP__dev_acarbose 2026-07-10 kind=geography_stage verify=M acarbose: 4 registered trial(s) in JP, highest phase 3 [NCT00221156] source NCT00221156 https://clinicaltrials.gov/study/NCT00221156 ctsearch__KR__dev_acarbose 2026-07-10 kind=geography_stage verify=M acarbose: 8 registered trial(s) in KR, highest phase 3 [NCT01514838] source NCT01514838 https://clinicaltrials.gov/study/NCT01514838 ctsearch__SG__dev_acarbose 2026-07-10 kind=geography_stage verify=M acarbose: 1 registered trial(s) in SG, highest phase ? [NCT00909051] source NCT00909051 https://clinicaltrials.gov/study/NCT00909051 nmpa__dev_acarbose__CN 2026-07-13 kind=geography_stage verify=M NMPA-approved in China (acarbose): 34 domestic approval(s) (e.g. Acarbose Tablets, 100mg, Zhejiang Jingxin Pharmaceutical, China); 1 imported approval(s). Reference NMPA H20244564. source NMPA:NMPA H20244564 https://www.nmpa.gov.cn/datasearch/home-index.html openfda__ANDA078470__US 2026-07-13 kind=geography_stage verify=M FDA-approved in the US (ACARBOSE); approved, marketed [ANDA078470] source ANDA078470 https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=ANDA078470