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NCT04160455: ATGALIG-HIV
Study of Autophagy and the Effects of GALIG Gene Products in HIV-1 Infected Patients Who Are Under Antiretroviral Therapy Since Primary-infection, Chronic Phase, or Never Treated.
trial testing expression of a panel in Autophagy in 180 participants. Currently enrolling.
7 November 2029
Quick facts
| Lead sponsor | Centre Hospitalier Régional d'Orléans |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 180 |
| Start date | 7 November 2019 |
| Primary completion | 7 November 2029 |
| Estimated completion | 7 November 2039 |
| Sites | 1 location across France |
Drugs / interventions tested
- expression of a panel — full drug profile →
Conditions studied
- Autophagy — all drugs for Autophagy →
- Galectins — all drugs for Galectins →
- HIV Infections — all drugs for HIV Infections →
- Highly Active Antiretroviral Therapy — all drugs for Highly Active Antiretroviral Therapy →
Sponsor
Centre Hospitalier Régional d'Orléans
Who can join
18 and older, any sex, with Autophagy or Galectins. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Little is known about autophagy during HIV infection. Recently, two different teams reported important dysfunctions of autophagy in HIV-infected patients despite sustained suppressive antiretroviral therapy. As altered autophagy is strongly linked to cellular senescence and chronic inflammation, two hallmarks of HIV-infected patients despite long-term suppressive antiretroviral therapy, it is important to improve our knowledge in the area. Our main objective is to determine whether all or part of mononuclear cell subpopulations (CD4+ and CD8+ T lymphocytes, and monocytes) exhibit a defect in autophagy function in a cohort of HIV-infected patients who are virologically-controlled (plasma HIV RNA \<50 copies / ml) either spontaneously (i.e. HIV controllers or post-treatment controllers) or after they started antiretroviral therapy at different time points (i.e. at the acute or chronic phases), as compared with a control group (i.e. uninfected healthy blood donors).
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Autophagy and Autophagy-Related Diseases: A Review.
Ichimiya T, Yamakawa T, Hirano T, Yokoyama Y, et al · · 2020 · cited 240× · PMID 33255983 · DOI 10.3390/ijms21238974 -
Multiple Facets of Autophagy and the Emerging Role of Alkylphosphocholines as Autophagy Modulators.
Kaleağasıoğlu F, Ali DM, Berger MR. · · 2020 · cited 26× · PMID 32410999 · DOI 10.3389/fphar.2020.00547 -
The Fragile Balance: Autophagy's Role in Neurodegenerative Disease Progression.
Bhushan B, Dhanawat M, Garima, Wilson K, et al · · 2026 · PMID 40619658 · DOI 10.2174/011570159x377552250627113915
Verify or expand the search:
- PubMed search for NCT04160455
- 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 NCT04160455 (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 Centre Hospitalier Régional d'Orléans
- Last refreshed: 30 December 2025
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/NCT04160455.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing