Study to Evaluate the Efficacy of MONotherapy of TiviCAY® Versus a Triple Therapy in HIV-1-infected Patients (MONCAY)

Centre Hospitalier Régional d'Orléans

Status and phase: Terminated; Phase 3

Conditions: HIV

Treatments: Drug: dolutegravir; Drug: dolutegravir 50mg +abacavir 600mg +lamivudine 300mg

Study type: Interventional

Funder types: Other

Identifiers

NCT02596334

CHRO 2015-03

Details and patient eligibility

About

Triple antiretroviral regimens have greatly improved the prognosis of patients living with HIV (PLHIV). Patients virologically controlled and having a good immune restoration can have a life expectancy close or equal to that of people not infected with HIV.[1] However, this is under the condition of a "lifetime" maintenance of an undetectable plasma viral load (pVL) (<50 cp/ml). On the other hand it is well established that aging increases comorbidities among PLHIV and the burden of co-medications.[2] This also has the consequence of frequent drug-drug interactions. In this context it is important to decrease pills burden, side-effects and drug-drug interactions, while maintaining undetectability.

Currently, there is a strong interest for medical research to validate lightened regimens (i.e. bithérapies [3-7] and monothérapies [8,9], particularly in a maintenance strategy, with the primary objective of reducing burden of pills and side effects. Several monotherapy trials using a boosted protease inhibitor (PI/r) showed high level of viral suppression, even if this proportion was not always non-inferior to maintaining a triple therapy. [8,9] Fortunately, when virological failure occurred under monotherapy virologic suppression was easily restored by the addition of two NRTI. Patients who are most likely to maintain viral suppression under a reduced scheme are those that have a high nadir (> 100 CD4 / mm3), no previous AIDS event and a sustained virologic suppression (>12 months).

Monotherapy is the option that best reduces the burden of pills and the risk of side effects or drug-drug interactions. It must be considered using very powerful molecule that harbor a strong binding to its ligand in order to minimize the risk of selecting resistant mutants in the case of virologic failure. To be as simple as possible in its use, it must be a single agent administered as a single dose once a day and not boosted if possible. The molecule must have very good tolerance. Finally, to be effective in viral sanctuaries this molecule should have a good (or sufficient) diffusion to ensure effective Cmin on wild viral strains. Dolutegravir meets all these exigences.[10] In addition, our team recently presented results of a pilot study showing that the switch of a successful combined antiretroviral regimen to dolutegravir monotherapy maintained undetectable viral load (<20 cp/ml) after a median of 7 months (range 6.5-10 months).

Enrollment: 158 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• HIV-1-infected patients with no previous AIDS event (excluding a healed tuberculosis);
• Current antiretroviral treatment associating dolutegravir + abacavir + lamivudine for at least 1 month;
• Nadir CD4 ≥ 100/mm3;
• Plasma RNA viral load < 50 copies/ml for at least 12 months;
• Plasma RNA viral load <20 or 40 copies/ml (according to the threshold of the method used by local laboratory) at the screening visit;
• No documented virologic failure or known resistance to any integrase inhibitor,
• Patient having provided a written consent;
• Patients follow-up possible in ambulatory;
• Patient age > 18 years;
• Covered by health insurance

Exclusion criteria

• Non-compliant patient

  • Subject is pregnant, or lactating, or of childbearing potential and without contraception;

  • Active opportunistic infections (defining AIDS);

  • Known hypersensibility to abacavir or lamivudine or dolutegravir;

  • Patients harboring HLA B*5701;

  • Major overweight (BMI ≥ 40);

  • Weight <40 kg;

  • Creatinine clearance < 50ml/min;

  • Cirrhosis or severe liver failure (factor V < 50%);

  • Life Prognosis threatened within 6 months;

  • Circumstances that may impair judgment or understanding of the information given to the patient;

  • Co-medication with carbamazepin, oxcarbamazepin, fosphenytoïn, phenobarbital, phenytoïn, primidon, St John's wort or dofetilid;

  • Malabsorption syndromes;

  • The following laboratory criteria:

    • Serum AST,ALT > 5 x upper limit of normal (ULN)
    • Thrombocytopenia with platelet count < 50.000/ml
    • Anemia with hemoglobin < 8g/dl
    • Polynuclear neutrophil count < 500/mm3

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

158 participants in 2 patient groups

triple therapy

Active Comparator group

Description:

dolutegravir + abacavir + lamivudine (TRIUMEQ) : oral administration, one tablet daily during 48 weeks.

Treatment:

Drug: dolutegravir 50mg +abacavir 600mg +lamivudine 300mg

monotherapy

Experimental group

Description:

dolutegravir (TIVICAY) : 50 mg, oral administration, one tablet daily during 48 weeks.

Treatment:

Drug: dolutegravir