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Open Label Rollover Study of Triumeq in Patients With Amyotrophic Lateral Sclerosis (ALS) Following the Lighthouse II Trial
Triumeq is an approved medicine for HIV. The effectiveness of Triumeq in Amyotrophic Lateral Sclerosis (ALS) is being investigated in the Lighthouse II trial. This study aims to assess whether Triumeq is safe and effective at delaying ALS disease progression when given long term. It is available for participants who have completed the Lighthouse II study. The main measurements are safety, tolerability and survival. The study will go for approximately 2 years.
Treatment options for ALS are very limited and there is a high unmet need for effective treatments. Triumeq targets a known neuron toxic pathway and is currently under investigation in a double blind placebo controlled trial, Lighthouse II. This study will be open to participants who took part in, and were still taking the study drug when they completed the Lighthouse II trial, in Australia and New Zealand. The nature of the target and the mechanism of action of Triumeq are well understood. Participation in this rollover study is concurrent with standard of care, so participants are not limited in their use of therapies. Participants will be assessed for adverse events, discontinuation of study medication, survival, measures of daily functioning, plus biomarker assessments of blood and urine samples. Participant contacts may be face to face, or remote, and will be at 3 monthly intervals until approx December 2026 by which time it is anticipated the results of the Lighthouse II study will be available.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Macquarie University, Neurology
North Ryde, New South Wales, Australia
Neuroscience Research Australia (NeuRA)
Randwick, New South Wales, Australia
Royal Brisbane and Womens Hospital
Herston, Queensland, Australia
Flinders Medical Centre
Bedford Park, S.A., Australia
Launceston General Hospital
Launceston, Tasmania, Australia
Calvary Health Care Bethlehem
Caulfield South, Victoria, Australia
The Perron Institute
Nedlands, W.A., Australia
Start Date
November 15, 2024
Primary Completion Date
June 3, 2025
Completion Date
June 3, 2025
Last Updated
June 8, 2025
12
ACTUAL participants
Abacavir 600mg, Lamivudine 300mg and Dolutegravir 50mg (Triumeq)
DRUG
Lead Sponsor
Macquarie University, Australia
NCT07483606
NCT04630392
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05901259