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NCT03986424: MIND
Local Study of Akatinol Memantine in VaD in Russia
Phase 3 trial testing Akatinol Memantine 20 mg in Vascular Dementia in 130 participants. Completed in 1 June 2022.
1 June 2022
Quick facts
| Lead sponsor | Merz Pharmaceuticals GmbH |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 130 |
| Start date | 23 January 2018 |
| Primary completion | 1 June 2022 |
| Estimated completion | 1 June 2022 |
| Sites | 4 locations across Russia |
Drugs / interventions tested
- Akatinol Memantine 20 mg — full drug profile →
- Akatinol Memantine 10 mg — full drug profile →
Conditions studied
- Vascular Dementia — all drugs for Vascular Dementia →
Sponsor
Merz Pharmaceuticals GmbH — full company profile →
Who can join
Adults 50 to 85, any sex, with Vascular Dementia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study evaluates the clinical efficacy and safety of Akatinol Memantine 20 mg (single-doses) vs. Akatinol Memantine 10 mg (double-doses) in patients suffering from moderate and moderately severe vascular dementia.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Clinical Trials of New Drugs for Vascular Cognitive Impairment and Vascular Dementia.
Linh TTD, Hsieh YC, Huang LK, Hu CJ. · · 2022 · cited 39× · PMID 36232368 · DOI 10.3390/ijms231911067 -
Mechanisms of mitophagy and oxidative stress in cerebral ischemia-reperfusion, vascular dementia, and Alzheimer's disease.
Lyu Y, Meng Z, Hu Y, Jiang B, et al · · 2024 · cited 19× · PMID 39169952 · DOI 10.3389/fnmol.2024.1394932
Verify or expand the search:
- PubMed search for NCT03986424
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Vascular Dementia
Currently open trials in the same condition.
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- NCT06416371 — Retinal Vessel Leakage in Cerebral Small Vessel Disease · recruiting
- NCT07259499 — Predictors of Emergency Department Use in Frail Patients · recruiting
Other Merz Pharmaceuticals GmbH trials
Trials by the same sponsor.
- NCT05585398 — A Study to Evaluate the Distribution of Botulinum Neurotoxin Type A Administered as Intradermal Injections, Comparing Di · Phase 1 · completed
- NCT04766723 — A Study to Investigate the Efficacy and Safety of NT 201 (Botulinum Toxin) Compared With Placebo for the Treatment of Ad · Phase 2 · completed
- NCT03256942 — Evaluation of the Sensitivity of Merz Lips Fullness Assessment Scale Following Etermis 4® Treatment for Lips Volume Augm · NA · completed
- NCT04210258 — Post-Market Clinical Follow-up Performance and Safety Study of Etermis 3 and 4 in the Face · completed
- NCT02270736 — Clinical Study to Investigate the Efficacy and Safety of NT 201 Compared to Placebo in the Treatment of Chronic Troubles · Phase 3 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03986424 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Merz Pharmaceuticals GmbH
- Last refreshed: 22 July 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03986424.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing