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Colchicine to Reduce Coronary Artery Inflammation in People With HIV (COLCOHIV)

A Randomised, Double-Blind, Multicenter, Placebo-Controlled Clinical Trial of Colchicine to Reduce Coronary Artery Inflammation in People With HIV. COLCOHIV

The purpose of this study is to evaluate whether colchicine can reduce coronary artery inflammation in people living with HIV and high cardiovascular risk. Participants will be randomized 1:1 to receive either colchicine or placebo for 96 weeks in a double-blind, multicenter clinical trial. Neither participants nor researchers will know which treatment is assigned during the study. The primary endpoint is the change in coronary artery inflammation measured by coronary computed tomography angiography (CCTA) after 96 weeks.

Panoramica dello studio

Descrizione dettagliata

Despite advances in antiretroviral therapy, people living with HIV (PWH) have an increased risk of cardiovascular disease compared with the general population. Persistent inflammation and immune activation are considered important contributors to accelerated atherosclerosis and coronary artery disease in this population. Coronary inflammation is associated with cardiovascular risk, but strategies targeting this mechanism in PWH remain limited.

Colchicine is an anti-inflammatory drug that has demonstrated cardiovascular benefits in patients with coronary artery disease by reducing inflammatory pathways involved in atherosclerosis. However, the effect of colchicine on coronary artery inflammation in PWH has not been previously evaluated. The hypothesis of this study is that colchicine may reduce coronary artery inflammation in PWH with high cardiovascular risk.

This phase II, randomized, double-blind, multicenter, placebo-controlled trial will include approximately 90 participants who will receive colchicine or placebo for 96 weeks. Changes in coronary artery inflammation will be assessed using coronary computed tomography angiography (CCTA) and the perivascular fat attenuation index (FAI), a non-invasive imaging biomarker of vascular inflammation. The study will also evaluate safety and changes in cardiovascular and inflammatory markers during follow-up.

Tipo di studio

Interventistico

Iscrizione (Stimato)

90

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

      • Barcelona, Spagna
        • Reclutamento
        • Hospital Universitario Vall d' Hebron
        • Contatto:
          • Alfonso Curran Fábregas, MD.
      • Madrid, Spagna, 28046
        • Reclutamento
        • Hospital La Paz
        • Contatto:
          • Jose Ignacio Bernardino de la Serna, MD.
      • Madrid, Spagna
        • Non ancora reclutamento
        • Fundación Jiménez Díaz
        • Contatto:
          • Alfonso Cabello Uceda, MD.
      • Madrid, Spagna
        • Non ancora reclutamento
        • Hospital Universitario de La Princesa
        • Contatto:
          • Lucio García Fraile, MD.

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • PWH > 50 years old
  • High cardiovascular risk measured by SCORE-2 > 5%
  • Stable antiretroviral therapy (ART) in the previous six months
  • Viral load < 50 copies/mililiter for at least 1 year. One blip is allowed (Viral load between 20-200 copies/mililiter with a previous and after viral load determinations < 20 copies per mililiter.
  • CD4 cell count > 350 cells/mm3
  • Stable dose of an intermediate or high intensity statin in the previous year (statin dose should not be modified throghout the study unless there is a robust clinical indication). In case the participant does not receive statins, all other hypolipemiants (bempedoic acid, ezetimibe) will need to be at a stable dose as well in the previous year.
  • No clinical indication for a change in treatment based on European Society of Cardiology Guidelines
  • Written informed consent obtained according to international guidelines and local laws
  • Ability to understand the nature of the trial and the trial related procedures and to comply with them

Exclusion Criteria:

  • Severe Heart failure defined as LVEF < 35%.
  • Previous MI, stroke or coronary by-pass surgery
  • History of non-cutaneus malignancy prior to enrollment
  • History of inflammatory bowel disease or chronic diarrhoea
  • Renal dysfunctions defined as eGFR < 50 ml/min or serum creatinine levels > 1.7 mg/dL
  • Severe hepatic impairments defined as a Child-Pugh category C
  • Participants with stomach ulcers or gastrointestinal bleeding
  • Levels of ALT over five times the upper limit of normal OR levels of ALT over three times the upper limit of normal AND bilirrubin levels over one point five times the upper limit of normal
  • Participant is receiving drugs that inhibit the CYP3A4 (e.g. Verapamil, Azithromycin, Clarithromycin, protease inhibitors, cobicistat), CYP2D6 or inhibitors of P-glycoprotein (see section 6.3.2 for more information)
  • Participant needs treatment with colchicine for any indication
  • Participants with highly elevated hsCRP > 10 mg/dL at screening
  • Women of childbearing potential. For this trial, definitions of nonchildbearing potential includes:
  • Permanent sterilisation methods including hysterectomy, bilateral salpingectomy and bilateral oophorectomy.
  • Postmenopausal state, defined as no menses for 12 months without an alternative medical cause. A high follicle stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a post-menopausal state in women not using hormonal contraception or hormonal replacement therapy. However in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient.
  • Male participants are considered fertile after puberty unless permanently sterile by bilateral orchiectomy. To prevent pregnancies in female partners of male participants, they must agree to use highly effective contraceptive methods or have practiced sexual abstinence during the treatment period and until the end of relevant systemic exposure, defined as 5 half-lives of the IMP (9 days approximately).
  • Known hypersensitivity to the active substances or any of the excipients
  • Known iodine contrast allergy with prior history of anaphylaxis
  • Patient without legal capacity who is unable to understand the nature, significance and consequences of the trial.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Study Group
Colchicine 0.5 mg orally once daily for 96 weeks.
Colchicine 0.5 mg administered orally once daily for 96 weeks as an anti-inflammatory treatment to reduce coronary artery inflammation in people living with HIV and high cardiovascular risk.
Comparatore placebo: Control Group
Matching placebo orally once daily for 96 weeks.
Matching placebo administered orally once daily for 96 weeks.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Changes in coronary artery inflammation
Lasso di tempo: Baseline to Week 96
Percent change from baseline of the mean Fat Attenuation Index (FAI) score for the three main coronary arteries (right coronary artery [RCA], left anterior descending artery [LAD], and left circumflex artery [LCX]). The mean FAI score will be calculated as the average of analyzable FAI scores with valid baseline and post-baseline measurements across the three coronary arteries.
Baseline to Week 96

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Changes in coronary plaque volume
Lasso di tempo: Baseline to Week 96
Change from baseline in total coronary plaque volume assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Changes in coronary plaque burden
Lasso di tempo: Baseline to Week 96
Change from baseline in coronary plaque burden assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in non-calcified plaque volume
Lasso di tempo: Baseline to Week 96
Change from baseline in non-calcified coronary plaque volume assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in mixed plaque volume
Lasso di tempo: Baseline to Week 96
Change from baseline in mixed coronary plaque volume assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in calcified plaque volume
Lasso di tempo: Baseline to Week 96
Change from baseline in calcified coronary plaque volume assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in prevalence of positive remodeling plaques
Lasso di tempo: Baseline to Week 96
Change from baseline in the percentage of coronary plaques presenting positive remodeling assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in prevalence of spotty calcium plaques
Lasso di tempo: Baseline to Week 96
Change from baseline in the percentage of coronary plaques presenting spotty calcium assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in prevalence of napkin-ring sign plaques
Lasso di tempo: Baseline to Week 96
Change from baseline in the percentage of coronary plaques presenting a napkin-ring sign assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in prevalence of low attenuation plaques
Lasso di tempo: Baseline to Week 96
Change from baseline in the percentage of coronary plaques presenting low attenuation characteristics assessed by coronary computed tomography angiography (CCTA) at Week 96.
Baseline to Week 96
Change in serum hsCRP concentration
Lasso di tempo: Baseline to Week 96
Change from baseline in serum high-sensitivity C-reactive protein (hsCRP) concentration at Week 96.
Baseline to Week 96
Change in serum IL-6 concentration
Lasso di tempo: Baseline to Week 96
Change from baseline in serum interleukin-6 (IL-6) concentration at Week 96.
Baseline to Week 96
Change in serum IL-1β concentration
Lasso di tempo: Baseline to Week 96
Change from baseline in serum interleukin-1 beta (IL-1β) concentration at Week 96.
Baseline to Week 96
Change in serum IL-18 concentration
Lasso di tempo: Baseline to Week 96
Change from baseline in serum interleukin-18 (IL-18) concentration at Week 96.
Baseline to Week 96
Change in serum SuPAR concentration
Lasso di tempo: Baseline to Week 96
Change from baseline in soluble urokinase plasminogen activator receptor (SuPAR) concentration at Week 96.
Baseline to Week 96
Change in extracellular vesicle NLRP3 levels
Lasso di tempo: Baseline to Week 96
Change from baseline in NLRP3 levels in extracellular vesicles at Week 96.
Baseline to Week 96
Change in extracellular vesicle ASC levels
Lasso di tempo: Baseline to Week 96
Change from baseline in ASC levels in extracellular vesicles at Week 96.
Baseline to Week 96
Change in extracellular vesicle Caspase-1 levels
Lasso di tempo: Baseline to Week 96
Change from baseline in Caspase-1 levels in extracellular vesicles at Week 96.
Baseline to Week 96
Change in classical monocyte proportion
Lasso di tempo: Baseline to Week 96
Change from baseline in the proportion of classical monocytes (CD14++CD16-) at Week 96.
Baseline to Week 96
Change in intermediate monocyte proportion
Lasso di tempo: Baseline to Week 96
Change from baseline in the proportion of intermediate monocytes (CD14+CD16+) at Week 96.
Baseline to Week 96
Change in non-classical monocyte proportion
Lasso di tempo: Baseline to Week 96
Change from baseline in the proportion of non-classical monocytes (CD14++CD16++) at Week 96.
Baseline to Week 96
Changes in leukocyte count
Lasso di tempo: Baseline to Week 96
Percentage change of leukocyte count in week 96
Baseline to Week 96
Changes in arterial inflammation in individual coronary vessels measured by Fat Attenuation Index (FAI)
Lasso di tempo: Baseline to Week 96
Change from baseline in FAI and FAI score, including mean absolute change and mean percent change, assessed in individual coronary vessels (right coronary artery [RCA], left anterior descending artery [LAD], and left circumflex artery [LCX]).
Baseline to Week 96
Mean arterial inflammation across analyzable coronary vessels measured by Fat Attenuation Index (FAI)
Lasso di tempo: Baseline to Week 96
Mean absolute change from baseline in mean FAI and FAI score calculated as the average of analyzable coronary vessels with valid baseline and post-baseline measurements.
Baseline to Week 96
Adverse events and serious adverse events
Lasso di tempo: Over the whole period of patient study participation
Incidence of solicited and unsolicited adverse events (AEs) and serious adverse events (SAEs) during the study.
Over the whole period of patient study participation

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Sex-related differences in inflammatory patterns and treatment response
Lasso di tempo: Baseline to Week 96
Difference in the percentage change of Fat Attenuation Index (FAI) between males and females in both treatment groups assessed by coronary computed tomography angiography (CCTA) in week 96.
Baseline to Week 96
CYP2D6 genotype-related differences in treatment response
Lasso di tempo: Baseline to Week 96
Difference in FAI percentage change according to CYP2D6 metabolizer classification in participants receiving colchicine.
Baseline to Week 96
Major adverse cardiovascular events (MACE)
Lasso di tempo: Baseline to Week 96
Difference in major adverse cardiovascular events (MACE) between colchicine and placebo groups assessed clinically in week 96.
Baseline to Week 96
Cardiovascular risk score
Lasso di tempo: Baseline to Week 96
Change from baseline in the CaRi-Heart risk score, including mean absolute change and mean percentage change.
Baseline to Week 96

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: José Ignacio Bernardino de la Serna, MD, PhD, Hospital Universitario La Paz. IdiPAZ

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 giugno 2026

Completamento primario (Stimato)

1 dicembre 2028

Completamento dello studio (Stimato)

1 giugno 2029

Date di iscrizione allo studio

Primo inviato

2 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 luglio 2026

Primo Inserito (Effettivo)

15 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

15 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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