WHO ICTRP trial
A phase III assessor-blinded randomised parallel group multi-centre study to…
EUCTR2010-019287-37-DE · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2010-019287-37-DE |
|---|---|
| Public title | A phase III assessor-blinded randomised parallel group multi-centre study to compare efficacy adn safety of two r-hFSH formulations (AFOLIA and Gonal-f®) in women for assisted reproductive treatment - not available |
| Scientific title | A phase III assessor-blinded randomised parallel group multi-centre study to compare efficacy adn safety of two r-hFSH formulations (AFOLIA and Gonal-f®) in women for assisted reproductive treatment - not available |
| Primary sponsor | Finox AG |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no |
| Countries | Spain;Denmark;Austria;Germany;United Kingdom |
| Conditions | Stimulation of multifollicular develoment in patients undergoing assisted reproductivet treatment |
| Interventions | Product Name: AFOLIA Product Code: not applicable Pharmaceutical Form: Solution for injection INN or Proposed INN: Follitropin alfa CAS Number: n.a. Current Sponsor code: human follicle stimulating hormone Other descriptive name: n.a… |
| Registration date | Apr 22, 2010 |
| Target size | 393 |
| Secondary IDs | FIN3001;not available |
| Registry page | clinicaltrialsregister.eu |
At a glance
- Yes Results available
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About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: