#AANAM – Early Parkinson’s Therapy, UCB0599, Well Tolerated in Phase 1b Trial

#AANAM – Early Parkinson’s Therapy, UCB0599, Well Tolerated in Phase 1b Trial
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Editor’s note: The Parkinson’s News Today team is providing in-depth coverage of the 2021 Virtual AAN Annual Meeting, April 17–22. Go here to read the latest stories from the conference.

 

UCB’s experimental oral therapy UCB0599 was generally well tolerated in people with mild to moderate Parkinson’s disease and other age-related conditions, a Phase 1b clinical trial reported.

Along with its good pharmacokinetic profile, which tracks the therapy’s movement into, through, and out of the body, these findings support UCB0599’s further development as a potential therapy for these patients.

An 18-month Phase 2 trial, called ORCHESTRA (NCT04658186), is now recruiting early stage Parkinson’s patients at sites in the U.S., Canada, and the Netherlands to test UCB0599’s safety and effectiveness against a placebo. More information can be found here.

Phase 1b study data were presented by Johan Smit, PhD, a clinical pharmacologist at UCB involved in UCB0599’s development, through a poster at the 2021 American Academy of Neurology virtual meeting running through April 22.

The poster is titled “Results from a Phase 1b Study of UCB0599, an Orally Available, Brain-penetrant Inhibitor of Alpha-synuclein (ASYN) Misfolding in People Living with Parkinson’s Disease (PD).”

In Parkinson’s disease, nerve cell loss is mainly triggered by the toxic buildup of misfolded alpha-synuclein, a protein abundant in the brain and thought to help regulate nerve cell function and communication.

Developed by UCB under a license from Neuropore Therapies, UCB0599 is a small, orally available molecule designed to suppress alpha-synuclein misfolding, so as to ultimately slow disease progression.

It is able to cross the blood-brain barrier, a semipermeable membrane that prevents potentially harmful microorganisms and large molecules carried by the blood from reaching the brain. This membrane is often an obstacle for the efficient delivery of brain-targeting therapies.

Previous preclinical studies showed that UCB0599 effectively suppressed the earliest alpha synuclein-related events driving Parkinson’s disease, prompting the Phase 1b placebo-controlled trial, called UP0077, to evaluate the therapy’s safety, tolerability, and pharmacokinetics in Parkinson’s patients.

The study involved 31 adults (21 men and 10 women) with mild to moderate Parkinson’s disease (Hoehn-Yahr stage 1–3), with a median age of 69 (range, 46–80), who had been living with the disease for a median of 67 months (about 5.5 years). All had age-related conditions.

Participants were randomly assigned to an oral capsule of either 90 mg of UCB0599 (seven patients) or 180 mg of UCB0599 (14 patients), or to a placebo (10 patients) twice a day for 28 days.

Results showed that most patients, both in the UCB0599 group (81%) and the placebo group (70%), experienced an adverse event, most being mild to moderate in intensity.

Those most frequently reported in both groups included headache (33.3% of UCB0599-treated patients and 20% of those given a placebo) and kidney damage (9.5% in the UCB0599 group and 20% in the placebo group).

Both a headache following lumbar puncture and low blood pressure were reported in 9.5% of patients given UCB0599, while fainting occurred in 20% of the placebo group.

Treatment-related adverse events were reported in nine UCB0599-treated patients and three patients on a placebo, and one patient in the 360 mg UCB0599 group (180 mg twice daily) and one in the placebo group discontinued treatment due to adverse events.

Two people, one from each UCB0599 dose group, also experienced an adverse event of special interest: unspecified hypersensitivity, or an exaggerated or inappropriate immune reaction, and hives (not serious or severe in intensity).

Three serious adverse events occurred: fainting in the placebo group, and chronic kidney failure and non-cardiac chest pain in UCB0599-treated patients.

While most adverse events were deemed unrelated to UCB0599, hypersensitivity and kidney function “will be continuously and closely monitored in future trials,” Smit said.

“No UCB0599 dose effects were observed, neither on the frequency nor the intensity of [adverse events], and no consistent or clinically relevant treatment-related patterns were observed for lab, vital signs, or [electrocardiogram] findings,” he added.

Moreover, the therapy’s pharmacokinetic profile was consistent with that previously observed in healthy volunteers, and treatment exposure increased with dose, as expected, Smit noted.

“UCB0599 was generally well tolerated in a population living with Parkinson’s disease with age-related [health conditions],” and these Phase 1b findings “further support the investigation of UCB0599, including its potential to slow down Parkinson’s disease progression,” Smit said.

Data from the ongoing Phase 2 ORCHESTRA trial, which is enrolling up to 300 adults, ages 40 to 70, with early stage Parkinson’s (Hoehn and Yahr stage 2 or lower) and a diagnosis within two years of a first study visit, will help to clarify UCB0599’s potential as a treatment. The trial is expected to finish by October 2023.

Marta Figueiredo holds a master’s in evolutionary and developmental biology and a PhD in biomedical sciences from the University of Lisbon, Portugal. Her research is focused on the role of several signaling pathways in thymus and parathyroid glands embryonic development.
Total Posts: 208
Ana holds a PhD in Immunology from the University of Lisbon and worked as a postdoctoral researcher at Instituto de Medicina Molecular (iMM) in Lisbon, Portugal. She graduated with a BSc in Genetics from the University of Newcastle and received a Masters in Biomolecular Archaeology from the University of Manchester, England. After leaving the lab to pursue a career in Science Communication, she served as the Director of Science Communication at iMM.
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Marta Figueiredo holds a master’s in evolutionary and developmental biology and a PhD in biomedical sciences from the University of Lisbon, Portugal. Her research is focused on the role of several signaling pathways in thymus and parathyroid glands embryonic development.
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