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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.

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

90

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

      • Barcelona, Spanje
        • Werving
        • Hospital Universitario Vall d' Hebron
        • Contact:
          • Alfonso Curran Fábregas, MD.
      • Madrid, Spanje, 28046
        • Werving
        • Hospital La Paz
        • Contact:
          • Jose Ignacio Bernardino de la Serna, MD.
      • Madrid, Spanje
        • Nog niet aan het werven
        • Fundación Jiménez Díaz
        • Contact:
          • Alfonso Cabello Uceda, MD.
      • Madrid, Spanje
        • Nog niet aan het werven
        • Hospital Universitario de La Princesa
        • Contact:
          • Lucio García Fraile, MD.

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verdrievoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.
Placebo-vergelijker: Control Group
Matching placebo orally once daily for 96 weeks.
Matching placebo administered orally once daily for 96 weeks.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Changes in coronary artery inflammation
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Changes in coronary plaque volume
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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

Andere uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Sex-related differences in inflammatory patterns and treatment response
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

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

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

1 juni 2026

Primaire voltooiing (Geschat)

1 december 2028

Studie voltooiing (Geschat)

1 juni 2029

Studieregistratiedata

Eerst ingediend

2 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

14 juli 2026

Eerst geplaatst (Werkelijk)

15 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

15 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

14 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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