ODYSSEY clinical trial design: a randomised global study to evaluate the efficacy and safety of dolutegravir-based antiretroviral therapy in HIV-positive children, with nested pharmacokinetic sub-studies to evaluate pragmatic WHO-weight-band based dolutegravir dosing

Abstract

Background

Dolutegravir (DTG)-based antiretroviral therapy (ART) is highly effective and well-tolerated in adults and is rapidly being adopted globally. We describe the design of the ODYSSEY trial which evaluates the efficacy and safety of DTG-based ART compared with standard-of-care in children and adolescents. The ODYSSEY trial includes nested pharmacokinetic (PK) sub-studies which evaluated pragmatic World Health Organization (WHO) weight-band-based DTG dosing and opened recruitment to children < 14 kg while dosing was in development.

Methods

ODYSSEY (Once-daily DTG based ART in Young people vS. Standard thErapY) is an open-label, randomised, non-inferiority, basket trial comparing the efficacy and safety of DTG + 2 nucleos(t) ides (NRTIs) versus standard-of-care (SOC) in HIV-infected children < 18 years starting first-line ART (ODYSSEY A) or switching to second-line ART (ODYSSEY B). The primary endpoint is clinical or virological failure by 96 weeks.

Results

Between September 2016 and June 2018, 707 children weighing ≥14 kg were enrolled; including 311 ART-naïve children and 396 children starting second-line. 47% of children were enrolled in Uganda, 21% Zimbabwe, 20% South Africa, 9% Thailand, 4% Europe. 362 (51%) participants were male; median age [range] at enrolment was 12.2 years [2.9–18.0]. 82 (12%) children weighed 14 to < 20 kg, 135 (19%) 20 to < 25 kg, 206 (29%) 25 to < 35 kg, 284 (40%) ≥35 kg. 128 (18%) had WHO stage 3 and 60 (8%) WHO stage 4 disease. Challenges encountered include: (i) running the trial across high- to low-income countries with differing frequencies of standard-of-care viral load monitoring; (ii) evaluating pragmatic DTG dosing in PK sub-studies alongside FDA- and EMA-approved dosing and subsequently transitioning participants to new recommended doses; (iii) delays in dosing information for children weighing 3 to < 14 kg and rapid recruitment of ART-naïve older/heavier children, which led to capping recruitment of participants weighing ≥35 kg in ODYSSEY A and extending recruitment (above 700) to allow for ≥60 additional children weighing between 3 to < 14 kg with associated PK; (iv) a safety alert associated with DTG use during pregnancy, which required a review of the safety plan for adolescent girls.

Conclusions

By employing a basket design, to include ART-naïve and -experienced children, and nested PK sub-studies, the ODYSSEY trial efficiently evaluates multiple scientific questions regarding dosing and effectiveness of DTG-based ART in children.

Trial registration

NCT, NCT02259127, registered 7th October 2014; EUDRACT, 2014–002632-14, registered 18th June 2014 (https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-002632-14/ES); ISRCTN, ISRCTN91737921, registered 4th October 2014.

Background

World Health Organization (WHO) guidelines recommend immediate ART for all adults and children living with HIV [1]. Although there has been substantial recent improvement in coverage of antiretroviral therapy (ART), only half of children in need have access to ART, with the majority (> 80%) living in Sub-Saharan Africa [2, 3]. The most commonly used regimens for human immunodeficiency virus (HIV)-infected children are triple combination ART with a ritonavir boosted protease inhibitor (bPI) or a non-nucleoside reverse transcriptase inhibitor (NNRTI). However, virological suppression on these regimens is worse compared to adults [4, 5], oral formulations of boosted-lopinavir are very poorly tolerated and there are concerns regarding pre-treatment resistance to NNRTIs in vertically-infected children [6, 7]. In this context, there is a need for alternative first- and second-line regimens for children with formulations which are well tolerated, easy for health workers to prescribe and for care-givers to administer.

Dolutegravir (DTG) is a second-generation integrase inhibitor with the advantage of once-daily dosing, a good short-term safety profile, low pharmacokinetic (PK) variability, few drug-to-drug interactions, rapid and robust virological response, a distinct resistance profile from raltegravir, a high genetic barrier to resistance and high potency at a low milligram dose. Following adult Phase II/III trials [8,9,10,11,12], the ODYSSEY trial aims to evaluate the efficacy and safety of once-daily DTG-based ART compared with standard-of-care (SOC) in children and adolescents (< 18 years) starting first- or second-line ART in resource-limited and well-resourced settings. We hypothesise that DTG with 2 nucleos(t) ides reverse transcriptase inhibitors (NRTIs) will be non-inferior to SOC in terms of efficacy and superior in terms of toxicity profile. This paper describes the design of the ODYSSEY trial, which has evolved over time to include nested PK sub-studies to evaluate pragmatic WHO weight-band-based DTG dosing and to open recruitment to children < 14 kg while dosing was still in development.

Changing licensing and guidelines for Dolutegravir

When ODYSSEY opened in September 2016, the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) had licensed the adult DTG dose (50 mg film coated tablet (FCT)) in adolescents weighing ≥40 kg and the FDA had licensed DTG 35 mg FCT in children weighing between 30 and 40 kg. Additionally, data from the ongoing IMPAACT P1093, a paediatric Phase II/III dose-finding study, supported using DTG 25 mg FCT in children over 6 years weighing between 20 and 30 kg [13]. In February 2017, the EMA reduced the weight and age limits for children down to ≥15 kg and ≥ 6 years.

Supported by further emerging efficacy data in adults [14] and the low cost of DTG, a number of countries had procured DTG formulations for adults by the end of 2017 [4]. In May 2018, data from an unplanned analysis of a National Institutes of Health (NIH)-funded observational surveillance study of pregnancies in Botswana (TSEPAMO) suggested an increased risk of neural tube defects (NTD) in infants born to women who became pregnant while taking DTG (data from August 2014 through to March 2019 showed 5 cases of NTD in 1683 infants (0.3%), which compares to a risk of ~ 0.1% in infants born to women on non-DTG based regimens) [15,16,17]. WHO issued a statement advising of a potential DTG safety signal [18]. Despite this, in July 2018, in response to efficacy data and the increasing levels of pre-treatment ART resistance documented in low- and middle-income countries (LMICs), WHO updated its recommendations to include DTG-based ART as a preferred first-line regimen for HIV-positive individuals ≥6 years and ≥ 15 kg (with alternative options for females of child-bearing age not using effective contraception) [19]. Updated data from the TSEPAMO study suggested that any increased risk of NTDs is lower than originally reported [17, 20]. President’s Emergency Plan for AIDS Relief (PEPFAR) and other partners continue to encourage responsible rollout [21]. In their 2020 report, the Clinton Health Access Initiative (CHAI) predicted that DTG-based first-line regimens would have a 93% market share in LMICs by 2024 [21].

Paediatric DTG formulations lag behind the adult formulation significantly. Although paediatric film-coated formulations (10 mg FCT, 25 mg FCT) were approved by stringent regulatory authorities in the US and Europe in 2016–2017, they are still not available outside high resource countries. Paediatric dispersible tablets, having only been recently approved in the US, are not yet available in countries.

Methods

Study design, number of children, randomisation and follow-up

ODYSSEY is an open-label, multi-centre, randomised, non-inferiority, Phase II/III, 96-week basket trial, powered to evaluate DTG-based ART in 2 cohorts: ART-naïve children (ODYSSEY A) and children starting second-line (ODYSSEY B). Children (< 18 years) were recruited at sites located in Uganda, South Africa, Zimbabwe, Thailand, Portugal, Germany, Spain and the United Kingdom. A basket design allows for enrolment to occur to two (or more) cohorts simultaneously at the same clinical sites, thereby improving efficiency and minimizing time and costs [22]. At trial design we planned to randomise 700 children (310 in ODYSSEY A and 390 in ODYSSEY B) 1:1 to receive 2 NRTIs with DTG (DTG arm) or SOC (bPI-, NNRTI- or non-DTG INSTI-based ART; SOC arm) (Fig. 1). Randomisation of children was stratified by ODYSSEY A/ODYSSEY B, routine availability at site of resistance tests for children failing treatment, intended SOC (bPI/non-bPI ART) and intended NRTI backbone (both specified prior to randomisation). The randomisation list was prepared by the trial statistician using random permuted blocks and securely incorporated within the trial database. Randomisation of study participants was done via a web service accessed by site clinician or one of the coordinating trials units. Allocation was concealed until randomisation occurred after which allocation was open—i.e. clinicians and carers were aware of group assignment.

Fig. 1

Trial Schema. Note: 85 additional children weighing 3 to < 14 kg were randomised to DTG versus SOC and will be followed up for 96 weeks. Abbreviations: ART = Antiretroviral Therapy; NRTI=Nucleos(t) ide reverse transcriptase inhibitors; bPI = boosted-Protease Inhibitors; NNRTI=Non-nucleoside reverse-transcriptase inhibitors; INSTI=Integrase Inhibitors

As a result of delays in dosing information for children < 14 kg, the trial was modified before recruitment closed to allow for the inclusion of ≥60 additional children weighing 3 to < 14 kg at enrolment (including a minimum of 20 children in each of the three lower weight-bands: 3 to < 6 kg, 6 to < 10 kg, 10 to < 14 kg) with participation in a PK sub-study for those randomised to the DTG arm. Minimum targets of 20 per weight-band were based on requiring ≥8 evaluable PK curves per weight band in the DTG arm and clinical opinion regarding numbers required < 14 kg to assess alongside the children ≥14 kg. Total enrolment was increased to allow for these additional children. Follow-up for the main trial population continued until the last ≥14 kg child recruited completed 96 weeks; each of the additional children < 14 kg is being followed-up for 96 weeks from randomisation. Including these extra children takes advantage of the opportunity ODYSSEY offers for a randomised comparison of DTG versus SOC in these younger/lighter children. Concurrent recruitment of children 3 to < 14 kg alongside the children weighing ≥14 kg was allowed for with randomisation stratified by < 14 kg and ≥ 14 kg to protect the main trial population ≥ 14 kg where randomisation was preserved. Randomisation of children < 14 kg was further stratified by weight-band (3 to < 6 kg, 6 to < 10 kg, 10 to < 14 kg) and ODYSSEY A/ODYSSEY B. Our design was planned to be robust if any/all of the lower weight-bands had to be dropped from the randomised comparison. Sub-study data were reviewed in children < 14 kg by the Independent Data Monitoring Committee (IDMC) (safety, efficacy and PK data) and by the Trial Steering Committee, ViiV Healthcare and the Trial Management Group (safety and PK data in DTG arm); had DTG been discontinued in any weight-band for safety concerns, PK concentration levels or lack of efficacy, we would have been able to drop children recruited in the respective weight-band (DTG and SOC participants) from our treatment comparisons. We are also able to analyse and report data on children enrolled weighing ≥14 kg while data are still accumulating in the children < 14 kg.

Study population

Eligibility criteria for ODYSSEY have changed over time mostly to expand eligibility to younger/lighter children (Table 1). In the initial ODYSSEY protocol, children had to be over 6 years and weighing ≥20 kg to be eligible. Throughout the trial, eligibility in both arms was contingent on a confirmed DTG dose being available for a given age/weight-band (or eligibility for a PK sub-study). Delays in dosing information for children< 14 kg and fast enrolment of ART-naïve children ≥35 kg led to the decision to cap recruitment of ART naïve children ≥35 kg in July 2017. When we stopped screening children ≥35 kg for ODYSSEY A, 100/172 enrolled in A were ≥ 35 kg, with the majority (94/100) aged 12 years or over. Although no cap was included in the protocol, the Trial Management Group and oversight committees considered it important to increase numbers < 35 kg and to keep trial places for younger children.

Table 1 Participant Inclusion and Exclusion Criteria from Protocol Version 4.0 onwards

Treatment of patients

NRTI backbone and SOC third-agents are prescribed according to national guidelines. Planned treatment was recorded prior to randomisation which was stratified (for children ≥14 kg) by whether or not bPI would be offered as SOC and by NRTI backbone, to ensure treatment groups were balanced for these factors. In countries where drug resistance tests were routinely performed, it was recommended that at least one active NRTI was chosen. In countries where drug resistance tests were not routinely performed, it was recommended at least one NRTI was chosen with presumed preserved activity based on treatment history.

DTG dose by protocol version has changed over time (Table 2) and has been driven by new licensing information and emerging data from IMPAACT P1093 [24] and ODYSSEY PK sub-studies (see below).

Table 2 Dolutegravir dosing in odyssey main trial participants by protocol version^g

Primary and secondary endpoints

The primary endpoint for the trial is virological or clinical failure by 96 weeks, which is defined as the first occurrence of any of the following: 1) insufficient virological response, 2) virological failure (two consecutive viral load measures ≥400 c/ml with the first at/after week 36), 3) new or recurrent AIDS defining event (WHO 4) or severe WHO 3 event, adjudicated by an independent blinded endpoint review committee or 4) all-cause death. The primary comparison is DTG vs SOC in the combined trial population (first-line and second-line children combined); subpopulation analyses (ODYSSEY A and ODYSSEY B) are key secondary comparisons. The components of the primary composite endpoint (virological failure and clinical failure) are included as secondary endpoints in addition to other key outcomes (Table 3).

Table 3 Primary and secondary outcome measures in odyssey

Sample size calculations

A non-inferiority margin of 10–12% was chosen, in accordance with previous HIV treatment trials [25, 26]. Assuming a failure rate of 18% overall (first-line and second-line children combined) in the DTG arm and SOC arm by 96 weeks and allowing for 10% loss to follow-up, 700 children provide 90% power to exclude (at two-sided 5% significance level) a difference of more than 10% in the primary outcome between the two arms. Enrolling 310 first-line ART and 390 s-line ART children provide 80% power to exclude a difference of more than 12% between the DTG and SOC arms in both subgroups separately, assuming a failure rate of 15% in ART-naïve (based on previous trials [27]) and 20% in ART-experienced children with 10% loss to follow-up.

Sub-studies

PK sub-studies

Weight-band PK sub-studies were introduced in Protocol version 3.0 (March 2017) with the aim of simplifying doses (using WHO weight-bands with no age restrictions) and using DTG formulations planned for manufacturing by generic companies.

In the first sub-study, PK and safety data were collected on 33 children weighing 14 to < 25 kg on DTG 25 mg FCT (Table 4). Exposures were low compared to reference data in adults [28].

Table 4 Dolutegravir dosing in odyssey pk sub-study participants by protocol version

In the second sub-study, 28 children weighing 25 to < 40 kg had PK on their initial dose (25 mg or 35 mg FCT); they then switched to the adult 50 mg FCT dose and underwent further PK and safety monitoring (Table 4). Based on the results of this sub-study [23] and following ethics approval, all children in the main trial weighing ≥25 kg moved to the adult 50 mg FCT dose.

Based on the results of the first two sub-studies, children weighing 14 to < 20 kg were changed to DTG 25 mg dispersible tablets (5x5mg DT which have higher bioavailability than FCTs), and children weighing 20 to < 25 mg were changed to DTG 30 mg DT (6x5mg DT) or DTG 50 mg FCT, with further PK and safety monitoring. Data on children weighing 20 to < 25 mg taking the adult DTG 50 mg FCT also demonstrated appropriate PK profiles [29].

Following review of ODYSSEY PK sub-study results by the Pediatric Antiretroviral Working Group (PAWG) of the WHO, WHO paediatric dosing guidelines have been updated to allow children 20 to < 40 kg to receive the adult 50 mg FCT dose [19].

Recruitment of children weighing 3 to < 14 kg was initiated under protocol version 4.0 and children randomised to DTG completed PK assessments [30].

A TB-PK sub-study with a within-child cross-over design is also evaluating the PK of DTG co-administered with rifampicin in HIV/tuberculosis (TB) co-infected children. Children on DTG diagnosed with TB start on rifampicin (RIF) and receive BID DTG (doubled daily dose) for the duration of TB treatment, and 2 weeks following. The first PK is undertaken at the end of TB treatment; followed by a second PK on QD DTG (once daily) ≥4 weeks after RIF is stopped, to allow for a wash-out period [31].

An immunology/virology sub-study will explore mechanisms of CD4 reconstitution, immune activation, HIV reservoir and low-level viral replication in the DTG and SOC arms.

A qualitative sub-study is investigating how best to support young people to maintain optimal adherence to second-line treatment, using interviews and focus groups with a small proportion of participants and carers in ODYSSEY B [32]. Young people and caregivers’ understanding of the DTG pregnancy safety alert have also been explored.

A folate and vitamin B12 sub-study at Ugandan sites was added in protocol v5.0 following the concerns raised around an increased risk of NTDs in babies born to mothers on DTG at conception [18]. Red cell folate and vitamin B12 levels will be assayed in samples prospectively collected at week 96 or later and compared between trial arms; change in plasma folate levels between week 4 and baseline (using routinely collected stored samples) will also be compared between arms.

In addition to the sub-studies, Youth Trial Boards in Uganda, Zimbabwe, South Africa and the UK have been developed alongside ODYSSEY to allow for meaningful engagement and participation of adolescent patient representatives in paediatric clinical trials. To date, they have had input into patient information sheets, have developed tools for explaining the risks of DTG in pregnancy to young people, and have participated in the development of a WHO toolkit and WHO webinars on youth participation in research.

Study procedures

All participants are seen at screening, enrolment, week 4, 12 and every 12 weeks to the end of follow-up. Every visit includes a clinical assessment including height, weight (and adjustment of drug doses accordingly), change in HIV disease stage, clinical events, adverse events and an adherence assessment (Table 5). In protocol version 3.0, questionnaires assessing mood and sleep symptoms were added. CD4, CD8, biochemistry and haematology laboratory tests are done at baseline, 4 weeks, 24 weeks and then 24-weekly, with lipids and glucose measured at baseline and 48-weekly. At sites where viral load is routinely measured every 12–16 weeks, real-time viral loads are measured at screening, week 4, 12, 24 and then every 12 weeks. At other sites, a real-time viral load is measured at screening (unless one is available from the last 4 weeks) to confirm eligibility in ODYSSEY B participants; otherwise viral loads are done according to local routine practice, and plasma samples stored at the above time-points for retrospective testing. Retrospective viral load testing is done in batches, and results are not used for patient management; this ensures generalisability of the trial results to LMIC settings where viral load is measured only 6 or 12-monthly according to WHO [33] and national guidelines. All viral load results are reviewed during the trial by the IDMC and we aim to have results of batched testing up-to-date for each IDMC review.

Table 5 Clinical assessments undertaken and frequency of testing

Study organisation, governance and ethics

The sponsor of the trial is the Paediatric European Network for Treatment of AIDS (PENTA) Foundation (https://penta-id.org/). Management of the trial is delegated to the clinical trials units: Medical Research Council Clinical Trials Unit at UCL (MRC CTU at UCL), French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (INSERM-ANRS) and PHPT-UMI 174 in Thailand. The trial was submitted for approval by Research Ethics Committees/Institutional Review Boards and by all required regulatory authorities in each of the participating countries.

Statistical analysis plan

The primary analysis will take place after the last participant recruited weighing ≥14 kg has completed 96 weeks and all children ≥14 kg have had a study closeout visit and will only include data in children recruited weighing ≥14 kg. The cumulative probability of clinical or virological failure by week 96 will be compared in the DTG and SOC arms, using the intention-to-treat population, estimated by the Kaplan-Meier Method adjusting for stratification factors. If the upper limit of the confidence interval for the difference between arms is < 10%, DTG-based ART will be considered non-inferior to SOC.

The primary endpoint includes confirmed HIV RNA ≥ 400 c/ml at or after 36 weeks. Since sites with frequent real-time viral load testing are likely to confirm failure more quickly than sites testing 6-monthly or annually, to ensure consistency for this endpoint the date of next scheduled visit following the first HIV RNA ≥400 (using schedule from randomisation) will be used for time to first confirmed viral load measurement ≥400c/ml (primary endpoint failure date), rather than the date of the confirmatory measure. Sensitivity analyses will include defining failure at first of two consecutive HIV RNA ≥ 400 c/ml at or after 36 weeks.

A small number of participants were randomised with minor ineligibility reasons and were retained in the trial. A secondary analysis will be done in the per protocol population excluding participants who did not meet the eligibility criteria and censoring follow-up at any change to the third agent (i.e. a change in either an INSTI, a PI, or an NNRTI, including adding an additional third agent or stopping treatment for > 31 days) for toxicity, failure or pregnancy/planned pregnancy.

Participants with VL < 50 (or < 400) c/ml at 48 and 96 weeks will be compared between arms based on (i) crude proportions and (ii) using the FDA snapshot algorithm. Change in total cholesterol, triglycerides and lipid fractions (LDL, HDL) from baseline to weeks 48 and 96 will be analysed using analysis of covariance to compare the change in mean level between the two arms, adjusting for baseline value and stratification factors. Other endpoints will be assessed using appropriate statistical methods.

There will be a secondary analysis of primary and secondary endpoints in children recruited weighing < 14 kg when this group has completed 96 weeks follow-up. Bayesian estimation will be used to report the primary endpoint, incorporating evidence obtained from participants enrolled ≥14 kg as a prior distribution. Clinical opinion has been elicited on the relative weight to allocate to the prior distribution [34]. The Bayesian analysis will be reported alongside frequentist analyses of the < 14 kg participants and of the whole trial population (< and ≥ 14 kg).

Results

Challenges in study implementation- changing landscape of DTG dosing

As described above, eligibility to ODYSSEY has expanded since the trial began to include younger/lighter children and DTG doses have been tested and modified within weight-bands, with protocol amendments, based on the PK sub-study results [23, 29] and with IDMC, TSC and ethics approval. This has increased the complexity of the trial for trial teams, particularly at PK sites. Drug supply management has also been challenging, to ensure correct DTG formulations are available at clinical centres in a timely manner.

The impact of using different DTG dosing within the same weight-band on the main trial comparison has been considered. We have taken the view that the trial will be a pragmatic comparison of DTG vs SOC for clinical or virological failure, and consider that it is more valuable to collect follow-up information on the doses likely to be licensed and used, particularly in low-resource settings.

Challenges in study implementation- pregnancy alert

The following measures were in place for girls of childbearing age prior to the DTG safety alert reporting a possible association between becoming pregnant on DTG and an increased risk of neural tube defect in the infant [15]:

• Eligibility contingent on negative pregnancy test and adherence to effective methods of contraception (Table 1)

• A pregnancy test every 24 weeks

• Pregnancies in trial participants reported, and outcomes followed-up

• Clinician discretion with respect to continuing DTG during pregnancy, with advice to consider alternative ART.

Following the safety alert, the trial team took the following actions:

• Participants were notified of this potential safety risk, prioritising those ≥15 years.

• Patient information sheets and consent forms were updated

• Availability of contraception and contraceptive counselling at each site was reviewed, and strengthened if necessary. Case report forms were revised to collect information about use of contraceptives.

• Participants in the DTG arm who have a positive pregnancy test within 8 weeks of their last menstrual period or who wish to become pregnant are now advised to switch to a non-DTG ART regimen in consultation with their clinician.

• The frequency of pregnancy testing for girls of childbearing age was increased to every (12-weekly) follow-up visit.

• Collection of data on use of folate supplements (advised during pregnancy) was strengthened.

• Youth Trial Board members created adolescent-friendly information on the safety alert, which can be provided to trial participants.

Post-trial access to DTG

Adult DTG (50 mg FCT) has been registered in all participating countries and is widely available in Europe and Africa. DTG DT formulations are unlikely to be available by the end of the trial. Protocol v6.0 includes extended observational follow-up for children in Africa and Thailand in both trial arms for a further 3 years; children on DTG at the end of the trial who continue in follow-up will be provided with DTG DT and (in Thailand) 50 mg FCT through ViiV Healthcare as necessary.

Current status of the trial

Between 20th September 2016 and 22nd June 2018, 707 children ≥14 kg were enrolled, including 311 ART-naïve children and 396 children starting second-line; enrolment was then closed to children ≥14 kg. Table 6 describes the baseline characteristics of children enrolled ≥14 kg: 621 (88%) have been enrolled in Africa; median (range) age was 12.2 [2.9–18.0]; 128 (18%) had WHO stage 3 and 60 (8%) WHO stage 4 disease; the majority were vertically infected. SOC is primarily efavirenz-based for ART-naïve children and lopinavir/ritonavir-based for ART-experienced children with abacavir+lamivudine or tenofovir+lamivudine/emtricitabine. Children recruited ≥14 kg all reached 96 weeks follow-up by end April 2020, with primary results expected by early 2021. Recruitment of children weighing 3 to < 14 kg started 5th July 2018 and completed 26th August 2019; 85 children were recruited, all in African sites, including 23 weighing 3 to < 6 kg, 39 weighing 6 to < 10 kg and 23 weighing 10 to < 14 kg at enrolment.

Table 6 Baseline characteristics of odyssey participants ≥14 kg at randomisation

Discussions

The ODYSSEY trial is an ambitious trial which has recruited HIV-infected children across 29 sites in 8 countries to evaluate DTG-based ART versus SOC. Recruitment of ≥700 children was completed ahead of target and an additional 85 children < 14 kg were recruited over 13 months. ODYSSEY employs a basket design to include ART-naïve and ART-experienced children, and, although the primary comparison will be in all children, the trial is powered to evaluate non-inferiority of DTG vs SOC in both sub-groups. To ensure relevance of findings across sub-Saharan Africa, where most HIV-infected children live, national guidelines are adhered to for real-time viral load testing and retrospective viral load testing is used to determine the trial’s virological outcomes.

When ODYSSEY was planned it was assumed that DTG dosing within the trial would follow recommendations arising from the IMPAACT P1093 paediatric DTG dosing study. In reality, dosing information became available slower than expected, while recruitment to ODYSSEY was faster than expected. In response, ODYSSEY included several nested PK sub-studies to allow recruitment of young children in the three lower weight bands. Pragmatic (WHO weight band-based) paediatric dosing using minimum formulations was assessed across the PK substudies aiming to simplify future procurement of paediatric formulations. Evaluation of adult DTG dosing down to children weighing 20 kg was incorporated, with the goal of enabling rapid access of DTG for the majority of children and easier implementation within LMICs national treatment programmes.

The advantages of nested PK in a larger trial translate into faster recruitment into PK studies and the generation of long-term safety data. Already, PK and safety data from ODYSSEY on the use of the adult DTG 50 mg FCT in children weighing ≥20 kg have been incorporated into WHO dosing guidelines [19]. WHO has predicted that this approach of conducting a parallel dose finding study (IMPAACT P1093) with a long term efficacy, safety and simplified dosing study (ODYSSEY) will likely result in ~ 500,000 children that can start or switch to DTG 3 years earlier than would otherwise have been possible [36].

Recruitment of children < 14 kg will provide valuable efficacy and safety data in this group. This was allowed for in a protocol amendment, with randomisation stratified to protect the main trial. Data from the weight-band PK sub-studies were included as part of FDA and EMA licensing applications for TIVICAY™ submitted by ViiV Healthcare and GlaxoSmithKline; with FDA approval for paediatric DTG received in June 2020 and EMA approval expected early 2021.

Conclusions

As identified by the WHO and the Collaborative Initiative for Pediatric HIV Education and Research (CIPHER), we must urgently accelerate the paediatric HIV response with evidence-based interventions to maximize short- and long-term outcomes in children. Through responsive and innovative design features, the ODYSSEY trial is contributing to this global research agenda, by efficiently answering multiple research questions around use of DTG in paediatric HIV care.

Appendix

Table 7 Severe who clinical stage 3 for the odyssey trial