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NCT03032315
Compare the Pharmacokinetics of TAH(80/10/12.5) Tablet in Comparison to the Co-administration of Telmisartan, Amlodipine and Hydrochlorothiazide in Healthy Male Volunteers
Phase 1 trial testing TAH Tablet (Telmisartan80/Amlodipine besylate10/Hydrochlorothiazide12.5) in Healthy in 44 participants. Completed in 27 December 2016.
27 December 2016
Quick facts
| Lead sponsor | IlDong Pharmaceutical Co Ltd |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 44 |
| Start date | 1 October 2016 |
| Primary completion | 27 December 2016 |
| Estimated completion | 27 December 2016 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- TAH Tablet (Telmisartan80/Amlodipine besylate10/Hydrochlorothiazide12.5) — full drug profile →
- TWYNSTA(Telmisartan+Amlodipine besylate) — full drug profile →
- Hydrochlorothiazide (hydrochlorothiazide) — full drug profile →
Conditions studied
- Healthy — all drugs for Healthy →
Sponsor
IlDong Pharmaceutical Co Ltd — full company profile →
Who can join
Adults 19 to 55, male only, with Healthy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
randomized, open-label, single dose, replicate crossover clinical trial to compare the pharmacokinetics of TAH(80/10/12.5) tablet in comparison to the co-administration of telmisartan, amlodipine and hydrochlorothiazide in healthy male volunteers
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03032315
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT03032315 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by IlDong Pharmaceutical Co Ltd
- Last refreshed: 26 January 2017
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/NCT03032315.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing