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Completed

NCT Number: NCT03320174

Long-Term Safety Study of Tafenoquine

This randomized, double-blind, placebo controlled study will involve 600 healthy (Glucose-6-Phosphate Dehydrogenase [G6PD] normal) volunteers. Participants who meet the eligibility criteria will be randomized (ratio 1:1) to receive a loading dose of either tafenoquine 200 mg (2 x 100 mg tablets) or placebo daily for three consecutive days, followed by study treatment (tafenoquine 200 mg or placebo) once per week for 51 weeks, with safety follow-up visits at Weeks 4, 12, 24, and 52. All participants will return to the clinic at Week 64 for an end of study visit. If the participant has an ongoing AE at the Week 64 visit will continue to be assessed for up to 3 more times at approximately 12-week intervals or until resolution or stabilization of the AE whichever is earlier.

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Key information

Conditions

Healthy Volunteers

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Linear Clinical Research, Nedlands, Western Australia, Australia

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Main Inclusion Criteria:

  • Completion of the written informed consent process (signed).
  • Male or female age 18 to 55 years inclusive, in good health as assessed by the Investigator.
  • Normal G6PD enzyme activity levels as defined by the parameters of the specific G6PD test employed at the local laboratory.
  • Negative HBsAg and HCV, HIV-1, HIV-2 antibody screen at the screening visit.
  • Negative serum pregnancy test.
  • Use acceptable method of birth control.
  • Hematology, biochemistry and urinalysis results at screening that are within the local laboratory reference range or, if outside the range, not clinically significant as judged by the Investigator in accordance with approved clinically acceptable laboratory ranges, documented prior to study start.
  • Willing and able to comply with all scheduled visits, treatment plan, laboratory tests, and other study procedures.

Main Exclusion Criteria:

  • History of allergy or intolerance to tafenoquine, primaquine or any excipients.
  • History of thalassemia or current or past history of methemoglobinemia or methemoglobin >2% at screening.
  • History of eye disease or surgery
  • Having previously received hydroxychloroquine for skin conditions or rheumatological diseases, chloroquine for malaria, tamoxifen, amiodarone or other drugs that may affect the optic nerve/retina/cornea within 30 days or 5 half-lives (whichever is longer) of study start. There are no travel restrictions, but the choice of concurrent anti-malarial must be atovaquone-proguanil if the participant chooses to take a registered antimalarial drug while travelling.
  • Any current diagnosis of Axis I psychiatric disorders

Treatment and study plan

Tafenoquine

Drug

Tafenoquine 200mg

Placebo

Other

Placebo

Primary outcomes

  1. Serious Ophthalmic Safety Event

    Time frame: After 12 months of exposure to study drug

    Number of Participants with One or More protocol-defined serious ophthalmic safety event (SOSE) assessed by retinal changes from baseline using SD-OCT and qFAF. SOSE is assessed by significant retinal changes from baseline using SD-OCT and qFAF.

Secondary outcomes

  1. Number of Participants With Mean Change From Baseline in Key SD OCT Parameters

    Time frame: After 12 months of exposure to study drug

    Mean change from baseline in key SD OCT parameters including central subfield thickness, total macular volume, and parafoveal (inner ring of Early Treatment Diabetic Retinopathy Study, and retinal thickness.

    Clinically significant change from baseline for central subfield thickness [change from baseline of at least 40 µm (15% change)].

    Clinically significant change from baseline for total macular volume [change of > 10% (0.86 mm3) from baseline].

    Clinically significant change from baseline for parafoveal (inner ring) retinal thickness [change from baseline of at least 10 µm].

    Clinically significant change from baseline for qFAF (change in mid-ring qFAF unit from baseline of at least 12% in both eyes at the same visit).

  2. Number of Participants With Ellipsoid or Interdigitating Zone Disruption

    Time frame: After 12 months of exposure to study drug

    Any ellipsoid or interdigitating zone disruption within the ETDRS grid

  3. Number of Participants With Mean Change From Baseline in Best Corrected Visual Acuity

    Time frame: After 12 months of exposure to study drug

    Mean change from baseline in BCVA score, the number of participants that have any clinically significant change in ETDRS BCVA (defined as ≥15 letter change [≥ 3 lines] of change in ETDRS BCVA at 4 meters).

  4. Number of Participants With Corneal Deposits From Slit Lamp Examination of the Corneal Epithelium

    Time frame: After 12 months of exposure to study drug

    Slit lamp examination was use to detect and grade corneal deposits (also known as vortex keratopathy or cornea verticillata) and retinal abnormalities arising from drug-induced phospholipidosis.

  5. Number of Participants With New Abnormalities Compared With Baseline Observed With Color Retinal Digital Photography

    Time frame: After 12 months of exposure to study drug

    Corneal deposits as determined by digital corneal photographs that are indicative of cornea verticillata also known as vortex keratopathy

  6. Number of Participants With New Abnormalities Compared With Baseline Observed With Microperimetry

    Time frame: After 12 months of exposure to study drug

    Microperimetry can be a useful tool for objective evaluation of macular function and progression of disease. Macular disease causes impairment of central vision, metamorphopsia, macropsia, micropsia and color vision defect. Microperimetry measures fixation stability which is associated with visual acuity.

  7. Number of Participants With Any Clinically Significant Change in ETDRS BCVA (Defined as >15 Letter Change [≥ 3 Lines] of Change in ETDRS BCVA at 4 Meters)

    Time frame: After 12 months of exposure to study drug

    Visual acuity was measured in a consistent way in order to detect any changes in vision as described in the Ophthalmic Reference Manual using a set of Early Treatment Diabetic Retinopathy Study (ETDRS) charts and a retro-illuminated box providing standardized illumination. Subjects are seated 4 meters from the letter chart and asked to read the letters. Letters read correctly count towards the total score. In addition, there are 5 letters in each of the 14 lines. The lines are of equal difficulty and follow a logarithmic progression of diminishing letter size related to the minimum angle of resolution. The endpoints include mean change from baseline in BCVA score, the proportion of participants that have any clinically significant change in ETDRS BCVA (defined as ≥15 letter change [≥ 3 lines] of change in ETDRS BCVA at 4 meters).

  8. Proportion of Participants Who Develop a Color Deficiency Using the Farnsworth-Munsell 100 (FM-100) Hue Test

    Time frame: After 12 months of exposure to study drug

    Color deficiency was assessed using the Farnsworth-Munsell 100 (FM-100) hue test

  9. Number of Participants Who Develop a Loss of 0.12 or Greater Logarithm of Contrast Sensitivity (logCS) on the Mars Letter Contrast Sensitivity Test

    Time frame: After 12 months of exposure to study drug

    The Mars letter contrast sensitivity test is a set of charts for testing peak visual contrast sensitivity. Subjects are asked to read to letters from left to right across the chart. The logarithm of contrast sensitivity (logCS) score is given by the log contrast sensitivity value at the lowest contrast letter just prior to two incorrectly identified letters, minus a scoring correction.

  10. Number of Participants Who Develop a Psychiatric Disorder in Accordance With DSM-5 as Assessed With the Mini International Neuropsychiatric Interview (M.I.N.I.) 7.0.2 Assessment Questionnaire

    Time frame: After 12 months of exposure to study drug

    Psychiatric disorders were reported as adverse events

  11. Number of Participants With an AE of Dizziness or Vertigo and Severity as Assessed by the Dizziness Handicap Inventory

    Time frame: After 12 months of exposure to study drug

    The period of observation for collection of AEs extended from the time of dosing (Day 1, Week 1 [Visit 2]) through the Week 64 follow-up visit. Proportion of participants with an AE of dizziness or vertigo are reported here.

Sponsors and collaborators

Lead sponsor

60 Degrees Pharmaceuticals LLC

Industry

Registry information

Official study title

Single Site, Randomized, Double Blind, Placebo-Controlled Study to Assess the Long-Term Safety of Tafenoquine

Important dates

Study start
2017
Primary completion
2021
Study completion
2021
First posted
Oct 25, 2017
Registry last updated
Apr 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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