Pegvaliase + Methotrexate for PKU
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to determine if combining methotrexate with Palynziq (pegvaliase) can help individuals with PKU better tolerate their treatment and enhance its effectiveness. PKU is a condition where the body cannot break down a specific amino acid, leading to health issues. The trial seeks adults who either have not tried Palynziq or have used it for at least 24 weeks without dose increases but still exhibit high levels of the amino acid in their blood. Participants must be in generally good health and willing to try both medications together. As a Phase 4 trial, this research focuses on understanding how this FDA-approved and effective treatment can benefit more patients.
Will I have to stop taking my current medications?
Participants must stop taking other PKU treatments besides Palynziq, as these are not allowed in the study.
What is the safety track record for Pegvaliase and Methotrexate?
Research has shown that pegvaliase is generally safe for humans, though it can cause some reactions. Approximately 72% of people using pegvaliase have experienced hypersensitivity reactions, which resemble allergic reactions but are less severe than anaphylaxis. These reactions vary among individuals, so managing them according to their severity is crucial. The FDA has approved pegvaliase to help adults with PKU lower their blood phenylalanine (Phe) levels, supporting its safety.
Methotrexate has undergone successful testing in humans, indicating a known safety profile. However, specific side effects when combined with pegvaliase are not detailed here.
Both treatments have established records of use, but like any medication, they may cause side effects. Clinical trial participants receive close monitoring to manage any reactions that occur.12345Why are researchers enthusiastic about this study treatment?
Most treatments for phenylketonuria (PKU) focus on strict dietary restrictions and enzyme replacement therapies like sapropterin dihydrochloride. But Pegvaliase, the study drug, works differently by using an enzyme called phenylalanine ammonia-lyase, which breaks down phenylalanine directly in the blood. This unique mechanism can significantly lower blood phenylalanine levels, which is crucial for patients who struggle to manage their condition with diet and existing therapies alone. Researchers are excited about combining Pegvaliase with Methotrexate because Methotrexate may enhance the tolerability and effectiveness of Pegvaliase, offering a potentially more robust treatment option for those with uncontrolled PKU.
What evidence suggests that this trial's treatments could be effective for PKU?
Research has shown that pegvaliase lowers blood phenylalanine (Phe) levels in people with phenylketonuria (PKU). In one study, 71.3% of adults using pegvaliase achieved safe Phe levels of 600 μmol/L or less. Another study found that adolescents experienced an average drop of 49.7% in their blood Phe levels. Among those using pegvaliase for extended periods, 87% saw a 20% reduction in Phe levels within a year, increasing to 93.5% after two years. This trial will evaluate the combination of pegvaliase with methotrexate. Participants in the "Palynziq naïve" arm will start with methotrexate alone before adding pegvaliase, while those in the "Palynziq experienced" arm will receive both treatments concurrently. This evidence supports pegvaliase's effectiveness in significantly reducing Phe levels in people with PKU.56789
Who Is on the Research Team?
Medical Director, MD
Principal Investigator
BioMarin Pharmaceutical
Are You a Good Fit for This Trial?
This trial is for adults aged 18-65 with phenylketonuria (PKU) who are in good health. Participants must be eligible and willing to take Palynziq and methotrexate, agree to use contraception if needed, carry two epinephrine devices during treatment, and either be new to Palynziq or have high blood levels despite ongoing treatment.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
MTX Tolerability Period
Participants receive MTX to assess tolerability before combination treatment
Combination Treatment Period
Participants receive concurrent MTX and Palynziq treatment
Follow-up Period
Participants continue with Palynziq only and are monitored for safety and effectiveness
What Are the Treatments Tested in This Trial?
Interventions
- Methotrexate
- Pegvaliase
Trial Overview
The study tests whether adding methotrexate can help reduce immune reactions and improve how well Palynziq works in adults with PKU. It includes people starting Palynziq for the first time or those not responding enough after long-term use.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Individuals with uncontrolled blood phenylalanine (Phe) \> 600 μmol/L on existing management who have never been treated with Palynziq. Participants will have a 4-week Screening Period, followed by a 4-week MTX Tolerability Period during which only MTX will be administered. If MTX is tolerated during the MTX Tolerability Period, the participant will then enter the 24-week Combination Treatment Period during which MTX + Palynziq will be administered concurrently. After completion of Week 24 (Combination Treatment Period), MTX will be discontinued for both cohorts and Palynziq only will continue for another 24 weeks (to Week 49).
Individuals who have uncontrolled blood Phe \> 600 μmol/L after ≥ 24 consecutive weeks of treatment with Palynziq, are on a current dose of ≥ 20mg/day and are unable to further dose escalate (Palynziq experienced). Participants will have a 4-week Screening Period. Participants will then have 24 weeks of concurrent MTX + Palynziq treatment (Combination Treatment Period): participants will be assessed for MTX tolerability during the first 4 weeks of MTX + Palynziq (MTX Tolerability Period) and then receive another 20 weeks of MTX + Palynziq. After completion of Week 24 (Combination Treatment Period), MTX will be discontinued for both cohorts and Palynziq only will continue for another 24 weeks (to Week 49).
Find a Clinic Near You
Who Is Running the Clinical Trial?
BioMarin Pharmaceutical
Lead Sponsor
Alexander Hardy
BioMarin Pharmaceutical
Chief Executive Officer since 2023
MBA from INSEAD
Greg Friberg
BioMarin Pharmaceutical
Chief Medical Officer
MD from New York Medical College
Citations
Long-term Comparative Effectiveness of Pegvaliase ...
Considerably more patients achieved blood Phe ≤600, ≤360, and ≤120 μmol/L and reductions from baseline of ≥20%, ≥30%, and ≥50% in blood Phe after 1 and 2 years ...
Pegvaliase + Methotrexate for PKU · Info for Participants
This Phase 4 medical study run by BioMarin Pharmaceutical needs participants to evaluate whether Pegvaliase will have tolerable side effects ...
3.
checkrare.com
checkrare.com/results-from-the-pegasus-clinical-trial-of-pegvaliase-in-patients-with-pku/Results From the PEGASUS Clinical Trial of Pegvaliase in ...
Results from the study show the ability of pegvaliase to significantly lower Phe compared to diet alone. At baseline, mean blood Phe was 1026.4 ...
Pegvaliase for the treatment of phenylketonuria: Final results ...
In 261 adult participants with a mean of 36.6 months of pegvaliase treatment, 71.3%, 65.1%, and 59.4% achieved clinically significant blood Phe levels of ≤600, ...
NCT05270837 | Study to Evaluate the Safety and Efficacy ...
This Phase 3 multicenter study is designed to evaluate the safety and efficacy of pegvaliase administered daily to adolescents (ages 12 to 17 years old (US), ...
Phenylketonuria (PKU) - StatPearls - NCBI Bookshelf - NIH
Phenylketonuria, also known as phenylalanine hydroxylase deficiency, is an inborn error of metabolism most commonly caused by pathogenic or ...
NCT05166161 | A Long-Term Safety Study of PTC923 in ...
The main purpose of this study is to evaluate the long-term safety of PTC923 in participants with phenylketonuria, and to evaluate the changes from baseline in ...
219666Orig1s000 INTEGRATED REVIEW - accessdata.fda.gov
The secondary safety data were provided by PKU-002 and PKU-004. The review team did not pool the safety data from PKU-002, PKU-. 003, and PKU ...
European guidelines on diagnosis and treatment of ...
The first European PKU guidelines advised 120–600 μmol/L as the target therapeutic range for patients aged ≥12 to 18 years [5,6]. This recommendation remains ...
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