A phase II open-label randomized controlled clinical trial.
To assess the efficacy of the following treatments for primary VL at day 28:
• the combination of single dose Liposomal amphotericin B® and a 10 day course of SSG
• the combination of single dose Liposomal amphotericin B® and a 10 day course of Miltefosine
• a 28 day course of Miltefosine
The areas of the two trial sites are endemic for VL. They are Dooka Hospital, Gedarif State, Sudan and Kimalel Hospital, Baringo district, Kenya. Addition of another Sudanese site will be considered. Data are brought to the Data Centre based at the study's Coordination Centre in Nairobi, Kenya. The trial is being conducted by the Leishmania East Africa Platform (LEAP: http://www.dndi.org/leap-platform
) in collaboration with the trial sites and is sponsored by the Drugs for Neglected Diseases initiative
The primary endpoint is initial cure, assessed at day 28 (figure ) based on clinical assessment and parasitologic evaluation (bone marrow or lymph node for Sudan and bone marrow or spleen aspirate for Kenya).
• Final cure, defined as the percentage of patients cured at day 210 (6 months follow-up) based on clinical evaluation, with parasitology done only if clinically indicated according to a standardised clinical assessment.
• Adverse events and serious adverse events occurring in the three study arms up to day 60.
• Description of the pharmacodynamic properties of all the three arms.
• Description of the pharmacokinetic properties of Miltefosine alone and in combination with Liposomal amphotericin B®.
Randomization sequences were generated, stratified by site in pre-determined block sizes by the Data Centre. Randomization codes have been concealed from investigators at the trial sites using sealed sequentially numbered, opaque envelopes. A copy of the randomization list is securely stored at the Data Centre. The envelopes are numbered sequentially externally. Inside each one there is a randomization sheet with the same sequential number as well as the treatment allocation. These randomization sheets are filed in the source documents which the monitor verifies at each site visit to confirm that only one envelope was opened for each patient to ensure integrity of the randomization process.
Liposomal amphotericin B® is being given as a single dose on day 1 at a dose of 10 mg/kg body weight infused in 5% dextrose running for 1-2 hours.
Miltefosine is being given orally at a dose of 2.5 mg/kg body weight daily, up to a maximum of 150 mg, for 28 days when used alone.
Miltefosine is being given orally at a dose of 2.5 mg/kg body weight daily, up to a maximum of 150 mg, for 10 days starting on day 2 following a single dose of Liposomal amphotericin B® 10 mg/kg.
SSG is being given IV/IM at a once daily dose of 20 mg/kg body weight daily for 10 days starting on day 2 following a single dose of Liposomal amphotericin B®.
Therefore the dose regimens is as follows
• Liposomal amphotericin B® one dose of 10 mg/kg body weight (IV) on day 1 followed by 10 days of SSG at 20 mg/kg body weight (IV/IM) from days 2-11.
• Liposomal amphotericin B® one dose of 10 mg/kg body weight (IV) on day 1 followed by 10 days of miltefosine at 2.5 mg/kg body weight (oral) from days 2-11.
• Monotherapy course of miltefosine at 2.5 mg/kg body weight (oral) from days 1-28.
All failure with compliance will be documented on the trial medication pages of the CRF.
Patients with clinical signs of VL (fever for at least 2 weeks and splenomegaly) and diagnosis confirmed by visualization of parasites in tissue samples on microscopy, aged between 7 and 60 years inclusive, signed written informed consent, negative HIV status.
Patients who have received any anti-leishmanial drugs in the last 6 months/relapse cases, negative lymph node/bone marrow or spleen smears, severe protein and or caloric malnutrition, previous history of hypersensitivity reaction to SSG or Amphotericin B, suffering from concomitant severe infection such as TB or other serious underlying disease which would preclude evaluation of patients response to study medication, suffering from other conditions associated with splenomegaly such as schistosomiasis, previous history of cardiac arrhythmia or an abnormal ECG, female of child bearing age (pregnant or lactating), haemoglobin <5 mg/dL, WBC <1 × 103/mm3, platelets <40,000/mm3, abnormal liver function tests (ALT and AST) of more than three times the upper limit of the normal range, serum creatinine outside the normal range for age and gender, major surgical intervention within two weeks prior to enrolment. These tests are standardised but it is not feasible to standardise routine clinical laboratory assessments as different machines and reagents are being used. However both internal and external QC will be carried out at both sites on a regular basis and training offered to site staff at the beginning and during the trial to ensure that the data collected are reliable and comparable.
HIV-status and VCT
All patients are offered counselling and screening for HIV (voluntary counselling and testing programme (VCT). This is done at the same time as consent is obtained for inclusion in the trial. Patients who decline VCT or are found to be HIV positive are not eligible to participate in this trial but receive appropriate treatment, according to national treatment guidelines. Additionally, they are referred onwards for treatment, surveillance and follow up according to the national protocol for HIV positive patients.
Standardised consent forms, adapted to the local context and translated into local languages and approved by ethics committees are being used. Signatures or thumbprints are obtained for consent, with witnesses in the latter case (illiterate subjects) for adults. In the case of children, the investigator gets their assent once permission of either the child's parent or guardian has been obtained.
Patients who do not meet inclusion criteria or who do not give consent are offered free treatment outside the trial, according to national treatment guidelines.
Analysis and sample size
Analysis of primary endpoint: cure at day 28
The study is designed and will be analyzed according to group-sequential methods, specifically the triangular test [10
]. Following the trials main objectives, the aim of the analysis is to efficiently identify a regimen that is a) inadequate, so its development can be discontinued, or b) adequate, so its development can proceed. In these terms, the highest efficacy (i.e. percentage of patients cured as per primary outcome) considered inadequate is set in this trial to be 75% (denoted p0
), and the lowest efficacy considered adequate as 90% (denoted pa
). The null and alternative hypotheses are H0
The triangular stopping boundary, as shown in Figure , was defined following Ranque et al [10
]. With both type I and type II error rates set at 5% (power 95%), and sequential analysis being done after every 15 patients per arm, the maximum sample size required is 189 (63 per arm). The actual sample size may be less than this, depending on when the actual percentage of patients cured leads to a boundary being crossed. The boundaries were calculated using custom-written functions in the R software [13
], having checked that they could reproduce the example in Ranque et al [10
Figure 2 Triangular region for study arms. Showing the boundaries for analyzing the sequential trial using the Triangular test with the following parameters (p0 = 0.75, pa = 0.9, α = 0.05, β = 0.05, and n = 10). The vertical line at n = 30 indicates (more ...)
Each analysis consists of calculating the quantities V (proportional to current sample size) and Z (number of observed minus expected treatment successes) and plotting them on Figure . Hence, for each arm, a line from the origin is plotted over time. Recruitment in an arm will be stopped when this line crosses either boundary of the triangular region. Crossing the lower or upper boundary means concluding inadequacy or adequacy, respectively. Since the three arms will be assessed separately, it is possible that one of them may be stopped prior to others.
The above procedure is subject to a constraint imposed for the PK component of the trial, which requires at least 30 patients in arms 2 and 3, subject to efficacy not being inadequate. Therefore, if the upper boundary is crossed at n = 15 (indicating adequate efficacy) that arm will be continued regardless until n = 30. However, if the lower boundary is crossed (indicating inadequate efficacy) at n = 15, then it will be stopped.
Crossing a boundary of the region implies that the percentage of patients cured is either greater than 90% (if the upper boundary is crossed) or no more than 75% (if the lower boundary is crossed). The maximum likelihood estimate of the efficacy, i.e. the number cured divided by the number of patients, is a biased estimator due to the sequential nature of the trial. To take this into account, the analysis will follow Bellissant et al [11
]. First, the sample quantity C*
will be calculated as
, where V*
is the terminal value of V
from the data sample, and the θa
parameter is the log-odds ratio θ
)) for p
. Then, the tables in Whitehead's Appendix A [12
] will be used to obtain the significance level of the test, and point and interval estimates of p
. The latter are provided in terms of factors by which to multiply θa
. Finally, these three values of θ
(i.e. point estimate and upper and lower confidence limits) will be transformed to corresponding sample values of p
-1)). Analysis will be done using STATA [14
Analysis of secondary endpoint: cure at day 210
The sequential analysis described above relates only to efficacy on day 28, not day 210. However, because the latter is likely to be highly correlated with the former, ignoring the sequential design in the latter analysis could give inconsistent results. For example, if the status of all patients is the same at day 210 as at day 28, then using different methods for analysis would give different efficacy estimates from the same data. This is because the day 28 estimate takes into account the sequential design which, in general, would differ from conventional analysis done on the same data at day 210.
Therefore, the day 210 efficacy will be estimated by considering it in terms of events over two consecutive time periods: up to day 28, and from day 28 to day 210. More specifically, the day 210 efficacy (i.e. percentage cured or p210) will be considered as the sum of two probabilities, as follows:
i) probability of being cured at day 28 and remaining cured at day 210.
ii) probability of not being cured at day 28 but becoming cured at day 210.
Each of these probabilities is the product of two terms and enables a point estimate of p210
r is the percentage of those people cured at day 28 who remain cured at day 210.
s is the percentage of those people not cured at day 28 who become cured at day 210.
The confidence interval will be estimated via the sampling variance of p210
. Using the 'delta method' [15
], this can be estimated as a function of the sampling variances of p28
; these three quantities being statistically independent. The sampling variance of p28
will be estimated as the square of its standard error, which in turn will be estimated as the width of its 95% confidence interval divided by 2 × 1.96, using a normal approximation. The sampling variances of r
will be estimated by considering them as standard binomial proportions.
The above procedure ensures that, for example, if no patients change cure status between day 28 and day 210 then the point estimates of p28 and p210 will be equal (because r = 1 and s = 0). The confidence intervals will, however, generally be unequal. This is because treating the progress between day 28 and day 210 as a separate variable implies additional sampling variation. For example, r has sampling variation even when equal to 1. Moreover, sampling variation is considered on the probability scale, not the log-odds scale as for p28. This also means that the calculated confidence interval could exceed the interval 0-1. In this case, it will be truncated at the limits of that interval.
When the analysis results in an arm being stopped, the final cure rate (day 210) will also be evaluated (when all those patients have reached that time point). If the point estimate of the day 210 cure rate is found to be <90%, then the arm (arm 1 & 2) will not be considered for further study (e.g phase 3).
Within each arm, the percentage cured at each time point will be presented by site. Chi-squared or Fisher's exact tests will be used to test for differences between sites in terms of primary and secondary efficacy endpoints at the 5% level of significance.
Schedule of Assessments and Expected Side Effects
Assessments are timed at days 0, 3, 7, 14, 21, 28, 60 and 210 (Table ) and include clinical, parasitology, haematology, biochemistry and pharmacokinetic assessments (table ). Baseline assessments include anthropometric, clinical and lab evaluations. Day 60 and 210 assessments require some flexibility on dates due to patient travel, visit windows for each is as follows- day 60 (+/- 10 days) and day 210 (+/- 21 days).
The decision to give rescue medication is based on a standard guideline for all trial sites. Any patient who receives rescue medication is considered a treatment failure at initial cure if receipt of rescue occurs on or prior to initial cure (day 28) and treatment failure at final cure if it occurs on or prior to final cure (day 210).
Rescue treatment to be given includes:
- Liposomal amphotericin B 30 mg/kg IV split into multiple doses (according to country protocol: Sudan - 3 mg/kg/day for 10 days)
- SSG 20 mg/kg IM for 30-60+ days: for patients not responding to initial rescue treatment or for patients requiring treatment for severe PKDL.
Post Kala-azar Dermal Leishmaniasis (PKDL)
A complication of Visceral Leishmaniasis, particularly in Sudan is post-Kala-azar Dermal Leishmaniasis (PKDL). PKDL is characterised by skin lesions which normally occur in the months following treatment in people who have recovered from VL. Patients are being monitored closely for PKDL at days 0, 28, 60 and 210. Diagnosis will be made clinically, based on the typical appearance and distribution of the rash.
Concomitant medication necessary for the health of the patient is permitted during the course of the study. Details of all concomitant medication taken during the study are recorded in the CRF with indication, daily dose, route and dates of administration.
The effects of VL disease and geographical differences on the pharmacokinetics (PK) of miltefosine remain largely unknown, with most available PK data coming from a relatively healthy European patient group with cutaneous leishmaniasis (CL) [16
]. A thorough PK study of miltefosine in adult VL patients has not been published, let alone in paediatric patients and no such data are available from the East-African region. This study will describe the pharmacokinetic profile of miltefosine in adults and children (>7 years of age) in both the monotherapy and combination therapy arm. Any significant PK interactions between liposomal amphotericin B and miltefosine will be assessed in the combination treatment arm.
Bioanalysis of miltefosine will be done on plasma samples with a volume of 50 to 250 μL taken during both treatment and follow-up (see table ), using a validated liquid chromatography tandem mass spectrometry (LC-MS/MS) assay for miltefosine [17
]. In children, a more sparse sampling strategy will be applied because of ethical concerns.
The PK of miltefosine will be modelled and analyzed using a population PK approach, which enables, for example the estimation of within- and between-subject variations. Non-linear mixed-effects modelling will be performed using the NONMEM statistical software package [18
]. The minimal value of the objective function (equal to minus twice the log likelihood) provided by NONMEM will be used as a goodness-of-fit characteristic, in addition to comparisons of standard errors of parameter estimates. Furthermore, performance of the models will be assessed via standard goodness-of-fit plots. Covariate models for body size will be evaluated stepwise to explain possible differences between paediatric and adult patients, including allometric or linear scaling of clearance and volume of distribution by either body weight or fat-free mass. The appropriateness of the covariate model will be evaluated by comparison of the objective function value given by NONMEM and resulting reduction in unexplained between-subject variability of the respective pharmacokinetic variables.
To assess treatment response during and after treatment, this study will apply repeated measurements of blood parasite loads using a real time reverse transcriptase polymerase chain reaction (qPCR) for L. donovani
in EDTA blood based on the amplification of single-stranded 18S rRNA as a pharmacodynamic (PD) marker [19
]. Differences in parasite clearance in the blood are to be expected between the treatment arms: combinations are likely to result in a more rapid elimination of Leishmania
parasites, hence the decreased duration of treatment. In this trial the blood parasite counts will be used as a PD marker of the parasite clearance rate and thus response to treatment.
In the arms receiving miltefosine, the outcome and parasite clearance measured by qPCR will be linked to miltefosine PK. Modelling of miltefosine PK/PD in our patients will enable us to establish variability in pharmacokinetics in relation to outcome, which is an essential component in the development of new treatment regimens.
All trial site staff; physicians, nurses, laboratory technicians and pharmacists received training on the study protocol, study specific procedures and International conference on harmonisation-good clinical practise (ICH-GCP) guidelines [21
]. Additional training sessions will be provided as required, using external consultants where necessary. Documentation of receipt of training is maintained at the Coordination Centre.
Quality control and quality assurance
Suitably qualified Clinical Monitors trained in GCP regularly visit trial sites to monitor all aspects of the trial including; informed consent procedures, drug accountability, source data verification, adverse event reporting, sample handling, analysis and secure data storage.
Data collection and data management
Data are to be recorded on 3-part no carbon required (NCR) case report forms (CRFs) by site investigators, transcribed from hospital source data. Unique patient identifiers, assigned at the time of randomisation, are linked to unique hospital record numbers. During monitoring visits, CRF data are cross-checked against hospital source data as much as possible by the monitor. The top sheet for each page of the CRF is brought to the central Data Centre for double-entry into GCP compliant open-access database software OpenClinica, version 2.7 [23
] with range checks implemented to detect unusual values at data entry, before analysis. Following validation, data will be read into Stata, version 11 special edition [14
] and pre-programmed command files will be used to generate lists of data value queries in a thorough data cross-checking process. Query forms are to be automatically generated via Microsoft Access©
database software and emailed to trial sites, copied to clinical monitors. The sites will print and make resolutions. At the next monitoring visit, monitors will verify resolutions and deliver to the Data Centre. Data corrections will be programmed in Stata to complete the data cleaning audit trail. At analysis, any unusual values detected would be verified with the investigator at the sites before final analysis is done to confirm correctness/completeness. This will also be captured in the data management report prior to database lock.
DNDi, as sponsor, will render all necessary assistance to investigators to ensure timely publication of results in an international peer-reviewed, for the benefit of patients and to inform national decision-making on VL treatment guidelines. Ancillary studies will acknowledge those involved by name where appropriate.
Trial site records will contain names and residential information for each patient to allow follow-up to take place. Only the unique numeric identifier assigned to patients will be extracted from patient records and transferred to the Data Centre. Patient data will be kept securely at trial sites under the responsibility of the site investigator.
During the course of the trial, site audits will be undertaken to assess compliance with ICH-GCP guidelines. Specific issues to be assessed include adherence to the protocol and standard operational procedures (SOPs), consent, laboratory practise, documentation and record keeping. All areas of non-compliance will be addressed by the site investigators or trial coordination centre depending on the findings.
Termination of the study
On approaching the end of planned recruitment, the trial coordination office will send written instructions by email to each site regarding the date to cease recruitment. All patients will be followed up as per the protocol, with the data being collected and cleaned. Once the data lock has been completed, site close out visits will be performed by the coordination team and clinical monitors. A decision for premature termination will be taken in consultation and agreement with the sponsor, investigators and the DSMB. All relevant ethics committees and regulatory authorities will also be informed of the reason for termination. Trial master files and completed CRFs will be archived by the coordination centre in Nairobi for 15 years.
Dissemination of Results
After recruiting 15 patients per arm, a brief interim analysis report presenting the efficacy, including the triangular analysis will be provided to the Data Safety Monitoring Board (DSMB) whose composition is based on WHO-TDR guidelines [24
]. The DSMB membership includes a pharmacologist, paediatrician and an epidemiologist. The DSMB will seek advice from an external statistician when necessary. This report will also contain a listing of serious adverse events occurring prior to the analysis date. Adverse event listings are to be provided at the request of the DSMB. The DSMB, through the Chair may request additional efficacy and safety data if they have concerns relating to trial conduct or other ethical and safety issues.
At the end of the trial, the clinical study report will be circulated to Principal Investigators, DSMB, Ethics Committees and Ministries of Health.
Ethical approval has been obtained from National and local Ethics Committees in Kenya and Sudan prior to the start of the trial in each Country. Ethical approval has also been granted by LSHTM Ethics Committee, the AMC Medical Ethics Committee issued a 'declaration of no objection'.
The DNDi Coordination Team, based mainly at the Coordination Centre, DNDi Africa, Kenya Medical Research Institute, Nairobi, are responsible for collation and submission of protocol amendments, organisation of training for trial staff, monitoring and supervision of trial conduct, day to day management of the trial, harvesting data collected at each site, trial monitoring visits and data management, all to GCP standards.