Celgosivir or Modipafant as Treatment for Adult Participants With Uncomplicated Dengue Fever in Singapore

• Status: Withdrawn
• Trial end date: 2019-08-08
• Target enrollment: 0
• Participant gender: All

Summary

Dengue fever is an acute febrile illness transmitted by mosquitoes, which affects half the world's population. There are 96 million symptomatic infections, 500,0000 hospitalisations and 25,000 deaths per year attributed to the disease. The economic burden is $12 billion. In Singapore, as elsewhere, the incidence of the disease continues to increase despite aggressive control measures. At present there are no approved medicines for treating dengue fever. Only supportive fluid replacement therapy is used to treat vascular leakage in patients with severe illness. Therefore there is an urgent need to find alternative treatments. Experiments in the laboratory have shown that Celgosivir and modipafant inhibit dengue virus and improve mouse survival. Both drugs have previously been used in humans with good safety records, so investigators are taking this one step further to find out how well it works in dengue patients. Investigators plan to enroll dengue patients within 48 hours of fever onset and assign them to one of four treatment groups over five days. Together with the support from the industry partner, 60°Pharmaceuticals PLC, the investigators will determine the safety and effectiveness of these drugs on acute dengue patients and pave the way forward for dengue antiviral medicines to reach patients.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Singapore General Hospital
• Collaborators: 60 Degrees Pharmaceuticals LLC; Duke-NUS Graduate Medical School

Criteria

Inclusion Criteria:

1. Male or female, aged 21-65 years;

2. Acute febrile illness with two or more manifestations (headache, retro-orbital pain, myalgia, arthralgia, rash, haemorrhagic manifestations, or leucopoenia) and occurrence at the same location and time as other confirmed cases of dengue fever;

3. Fever (> 37.5°C) or history of fever at screening

4. < 48 hours of fever history

5. Positive NS1 strip assay or reverse-transcriptase polymerase chain reaction (RT-PCR).

6. Able and willing to give written informed consent; and,

7. Willing to be an inpatient from Study Screening to Study Day 5 and to return to hospital on study Days 14 and 28.

8. Willing to keep a study diary from Study Day 5 to Day 14.

Exclusion Criteria:

1. Clinical signs and symptoms for severe dengue, such as:

• Severe abdominal pain;

• Persistent vomiting;

• CS fluid accumulation;

• Mucosal bleeding;

• Altered mental state;

• Liver enlargement > 2 cm;

• Systolic blood pressure < 90 mmHg; and

• Pulse pressure < 20 mmHg.

2. A person with any of the following laboratory values:

• Haematocrit >52% males; >46% females;

• Aspartate or alanine aminotransferase (AST or ALT) > 1000 U/L;

• Room air oxygen saturation < 95%;

• Absolute neutrophil count < 1500/µL;

• Platelet count < 80,000/mm3;

• Creatinine > 165 µmol/L males; > 130 µmol/L females;

• Haemoglobin < 13.0 g/dL males; < 11.0 g/dL females;

• Total bilirubin > 24 µmol/L; and

• Serum CPK > 600 U/L.

3. History of or presently active intestinal disorders such as peptic ulcers, intestinal ulcers, intestinal obstructions, intestinal hernias, ulcerative colitis, malabsorption syndrome, celiac disease, Roemheld's syndrome (gastroesophageal regurgitation disease) or Crohn's disease;

4. Severe diarrhoea (grade 2 or higher according to NIH clinical trial guidelines);

5. Current usage of any anticoagulant drugs including, but not limited to, aspirin, warfarin or clopidogrel;

6. Any other CS acute illness within seven days prior to first study drug administration;

7. History of adverse reactions to celgosivir, castanospermine, modipafant or formulation excipients or history of severe drug or food allergies;

8. Exposure to any new investigational drug within 30 days prior to the study drug administration;

9. CS abnormal physical examination unrelated to dengue infection, chest X-ray or 12-lead ECG at screening such as QTc prolongation (> 450 msec);

10. Women of child bearing potential (WOCBP) who are pregnant, breast feeding or unwilling to avoid pregnancy by the use of highly effective contraception (<1% failure rate per year) including oral and subcutaneous implantable hormonal contraceptives, condoms, diaphragm, or intra-uterine system (IUS), during the period that the experimental drug is administered. Prospective WOCBP must have a negative pregnancy test (point of care).

11. Male participants unwilling to comply with the contraceptive requirements of the study as detailed in Section 4.7 (i.e. abstinence, effective barrier contraception during the study and for 65 days after the last dose of study drug).

12. Current significant medical condition or illness including cardiac arrhythmias, cardiomyopathy or other cardiac disease, asthma or other respiratory disease, diabetes mellitus, renal or hepatic impairment, thyroid disease, Parkinson's disease, epilepsy or history of unexplained blackouts, immunocompromised state including known HIV infection, or any other illness that the Investigator considers should exclude the patient, especially those that require continuation of other medications likely to have an interaction with the study drug.

13. Any condition that would render the informed consent invalid, or limit the ability of the participant to comply with the study requirements.

14. Any condition that, in the opinion of the Investigator, would complicate or compromise the study or well-being of the participant.