Trial to Determine Efficacy of Fexinidazole in Visceral Leihmaniasis Patients in Sudan

Visceral Leishmaniasis Clinical Trial

Official title:

Phase II Proof of Concept Trial to Determine Efficacy of Fexinidazole in Visceral Leishmaniasis Patients in Sudan

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01980199
• Other study ID #: FEXI VL 001
• Status: Terminated
• Phase: Phase 2
• First received: November 4, 2013
• Last updated: October 29, 2015
• Start date: November 2013
• Est. completion date: September 2015

Study information

• Verified date: July 2014
• Source: Drugs for Neglected Diseases
• Contact: n/a
• Is FDA regulated: No
• Health authority: Sudan: National Medicines and Poisons Board
• Study type: Interventional

Clinical Trial Summary

This study is designed to determine the efficacy of Fexinidazole as an oral treatment in Visceral Leishmanisasis sudanese adults patients.

The results of this proof of concept study will allow to make a decision on whether to proceed with clinical development of Fexinidazole for visceral leishmaniasis.

Description:

Visceral Leishmaniasis (VL) is a neglected disease and it is fatal if left untreated.

Until recently the first line treatment in East Africa was 30 days of Sodium Stibogluconate which can be cardiotoxic. Since 2010 WHO recommended Sodium Stibogluconate and Paromomycin for 17 days which is a shorter treatment but there remains the toxicity associated with these drugs. The second line treatment is Ambisome given as 6-10 intravenous infusions, whilst this has a better safety profile than other VL regimens it is expensive.

So there is an urgent need for short course oral treatment for VL particularly in the East African region.

Fexinidazole is a 2 substituted 5-nitroimidazole formulated for oral administration. Fexinidazole through its metabolites has demonstrated potent activity againts L. donovani intracellular amastigotes in vitro and in vivo in a visceral leishmaniasis mouse model.

The dose selected for this study (1800 mg/1200 mg for 4/6 days) has been based on the dose selected for a phase II trial on Human African Trypasonomiasis. It is albeit well tolerated and is one dose level below the maximum tolerated dose level established in phase I.

The trial is designed and will be analysed according to a sequential method known as the triangular test, using day 28 data. This sequential design allows for repeated interim analysis (every 10 patients). The null hypothesis is that the proportion cured is less than or equal to 75%. The primary endpoint is initial cure at day 28. The primary population for interim analyses and interim decision making will be the per protocol population.In the final analysis of cumulative patient data, Intention to Treat and Per Protocol Population analyses will be conducted.

The conventional 6 months (day 210) follow up outcome is still an important secondary endpointfor the final decision on whether to proceed with clinical development of Fexinidazole for VL.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 14
• Est. completion date: September 2015
• Est. primary completion date: November 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 15 Years to 60 Years

Eligibility

Inclusion Criteria:

• Patients with clinical signs and symptoms of primary VL (fever for at least 2 weeks, splenomegaly) and diagnosis confirmed by visualization of parasites in tissue samples (lymph node, bone marrow) on microscopy.

• Patients aged between 15 and 60 years (inclusive) who are able to comply with the protocol.

• Patients for whom written informed consent has been signed by the patients themselves (if aged 18 years and over) or by parents(s) or legal guardian for patients under 18 years of age together with the patients assent.

• HIV negative status

Exclusion Criteria:

• Patients who have previously been diagnosed with VL and received anti-leishmanial treatment (ie relapse)

• Patients with BMI <16 kg/m2

• Patients with contra-indication (known hypersensitivity) to other imidazoles (e.g. ketaconazole)

• Patients suffering from a concomitant severe underlying disease (cardiac, renal, hepatic) including hepatitis B, para kala-azar dermal leishmaniasis and tuberculosis

• Patient with clinically significant ECG findings or QTcF= 450 msec in 2 successive ECGs

• Major surgical intervention 4 weeks prior to enrollment.

• Patients who are pregnant or lactating.

• Female patients of child bearing age who do not agree to use an acceptable method of contraception

• Patients with haemoglobin < 5g/dl.

• Patients with platelets < 40,000/mm³.

• Patients with liver function (ALT and AST) tests of more than 2 times the upper limit of the normal range.

• Patients with serum creatinine above the normal range for age and gender.

• Patients with serum potassium (K+) above the normal range

• Patients with Bilirubin more than 1.5 times the upper limit of the normal range

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Leishmaniasis
• Leishmaniasis, Visceral
• Visceral Leishmaniasis

Intervention

Drug:
• Fexinidazole
600 mg tablets given orally, after the main daily meal at the daily dose of 1800 mg (3 tablets) once a day for 4 days continued by 1200mg (2 tablets)once a day for 6 days

Locations

Country	Name	City	State
Sudan	Doka Hospital	Doka	Gedaref

Sponsors (1)

Lead Sponsor	Collaborator
Drugs for Neglected Diseases

Country where clinical trial is conducted

Sudan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Safety endpoint	Proportion of patients with SAE and/or AEs leading to treatment discontinuation	From first dose of trial medication to day 56 for non serious AEs and to day 210 for SAEs	Yes
Other	Safety endpoint	Proportion of patients experiencing at least one non-serious treatment emergent AE	From first dose of trial medication to day 56	Yes
Other	Pharmacokinetic assessment	Whole blood concentration of Fexinidazole and metabolites (sulfone and sulfoxide) in an intensive cohort of 10 patients (18 sampling time points) and in a regular cohort for all other patients (6 sampling time points)	From day 1 to day 12	No
Other	Pharmacodynamic assessment	Parasite load in blood and bone marrow (if remainder of bone marrow aspirate sample) to follow parasite clearance rate	Screening, D1, D3, D5, D8, D11, D14, D28, D56, D210	No
Primary	Initial cure	Proportion of patients with an abscence of parasites in tissue aspirate and no rescue treatment administered up to and including day 28	Day 28	No
Secondary	Final cure	Proportion of patients initially cured at day 28 (or day 56 for slow responders) with no further signs or symptoms of visceral leishmaniasis and no requirement for rescue medication during follow-up phase up to and including the day 210	Day 210	No