WHO ICTRP trial
Safety Assessment of 10-Day Daily Bucco-Oral Administration of Transfer Factor…
CTIS2024-511448-17-02 · EU Clinical Trials Information System · Not Recruiting
Key facts
| Trial ID | CTIS2024-511448-17-02 |
|---|---|
| Public title | Safety Assessment of 10-Day Daily Bucco-Oral Administration of Transfer Factor in Healthy Adult Human Subjects |
| Scientific title | - CPA 556-24 |
| Primary sponsor | Cepha s.r.o. |
| Secondary sponsors | Aumed a.s. |
| Registry | EU Clinical Trials Information System |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): Yes Therapeutic exploratory (Phase II): No Therapeutic confirmatory - (Phase III): No Therapeutic use - (Phase IV): No |
| Countries | Czechia |
| Conditions | healthy subjects, It is used in conditions with decreased immunity to enhance it e.g. in case of recurrent and chronic viral infections. MedDRA version: 20.1Level: LLTClassification code: 10000566Term: Acquired immunodeficiency syndrome… |
| Registration date | Aug 27, 2024 |
| Target size | 16 |
| Registry page | euclinicaltrials.eu |
At a glance
- Yes Results available
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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: