B-FREE Chronic Babesiosis Study

ID#: NCT06656351

Age: 18 years - 66+

Gender: All

Healthy Subjects: No

Study Phase: Phase 2

Recruitment Status: Recruiting

Start Date: November 18, 2025

End Date: September 01, 2027

Contact Information:
Core Research
212-241-7658
Summary: Phase 2 Open Label Study of Tafenoquine for Treatment of Chronic Babesiosis Patients with Severe Fatigue
Eligibility:

Inclusion Criteria:

- Male or female, aged ≥ 18 years

- Severe disabling fatigue

- Have at least one common symptom of babesiosis

- Have laboratory evidence of exposure to babesia in the last 12 months

- Able and willing to give written informed consent

- Able and willing to perform all study assessments

- If female negative urine pregnancy test and

- If female agree to use an acceptable method of birth control

Exclusion Criteria:

- Glucose-6-phosphate-dehydrogenase (G6PD) deficiency

- Breastfeeding

- Unmanaged Psychotic disorder

- Known hypersensitivity reaction to tafenoquine or other 8-aminoquinolines

- Current or planned treatment with quinine

- Uncontrolled cardiopulmonary or endocrine disorders

- Taking OCT2/MATE substrates without appropriate medical oversight

- Medical history of chronic, active viral diseases including HIV/AIDS, hepatitis B, and hepatitis C

- Have a risk factors for relapsing babesiosis

- Anorexia

- Any concomitant significant illness unrelated to babesiosis

- The patient is unable to tolerate medication by the oral route

- The patient has previously taken tafenoquine

- Hemoglobin at baseline is ≤ 8 g/dL