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NCT01793818: EVATAT
Evaluation on Seropositive Patients of a Synthetic Vaccine Targeting the HIV Tat Protein
Phase 1/Phase 2 trial testing Tat Oyi in AIDS in 50 participants. Status unknown.
1 March 2016
Quick facts
| Lead sponsor | BIOSANTECH |
|---|---|
| Phase | Phase 1/Phase 2 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 50 |
| Start date | 1 February 2013 |
| Primary completion | 1 March 2016 |
| Estimated completion | 1 March 2016 |
| Sites | 1 location across France |
Drugs / interventions tested
- Tat Oyi — full drug profile →
Conditions studied
- AIDS — all drugs for AIDS →
Sponsor
BIOSANTECH — full company profile →
Who can join
Adults 18 to 64, any sex, with AIDS. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Optimal vaccine dose (phase I/II)
Time frame: Two years
No undesirable events due to vaccination and viremia remaining \< 100 copies/ml after interruption of ART.
Sponsor's own description
Tat Oyi vaccination on seropositive patients could help their immune system to recognize and neutralize Tat. The neutralization of extra cellular Tat should help the cellular immune response to eliminate HIV-1 infected cells.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
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Current progress in the development of prophylactic and therapeutic vaccines.
Li T, Qian C, Gu Y, Zhang J, et al · · 2023 · cited 39× · PMID 36469218 · DOI 10.1007/s11427-022-2230-4 -
Intradermal injection of a Tat Oyi-based therapeutic HIV vaccine reduces of 1.5 log copies/mL the HIV RNA rebound median and no HIV DNA rebound following cART interruption in a phase I/II randomized controlled clinical trial.
Loret EP, Darque A, Jouve E, Loret EA, et al · · 2016 · cited 19× · PMID 27036656 · DOI 10.1186/s12977-016-0251-3 -
Perspectives for immunotherapy: which applications might achieve an HIV functional cure?
Vieillard V, Gharakhanian S, Lucar O, Katlama C, et al · · 2016 · cited 10× · PMID 26950274 · DOI 10.18632/oncotarget.7793
Verify or expand the search:
- PubMed search for NCT01793818
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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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 NCT01793818 (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 BIOSANTECH
- Last refreshed: 9 February 2016
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/NCT01793818.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing