Main clinical study

In our pivotal head-to-head study, RISE-PD, CREXONT gave people more “Good On” time with less frequent dosing compared to IR CD/LD*

Main clinical study

What is RISE-PD?

RISE-PD is a Phase 3, double-blind, head-to-head study that helped support FDA approval of CREXONT by exploring its benefits in people taking CREXONT compared to people taking IR CD/LD.

*“Good On” time is defined as “On” time without troublesome dyskinesia.

More “Good On” time

Explore the benefits of CREXONT

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MAIN MEASUREMENT

30 mins more “Good On” time with less frequent dosing

compared with IR CD/LD

“Good On” time is defined as “On” time without troublesome dyskinesia. Change in “Good On” time was measured by comparing values at the end of study to baseline; P=0.019 vs IR CD/LD.

This was the average dose frequency during the double-blind maintenance period.

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SECONDARY MEASUREMENT

30 mins less “Off” time per day§¶

compared with IR CD/LD

§This was a secondary endpoint of the study.

Study end=Week 20 or early termination; P=0.025 vs IR CD/LD.

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A DIFFERENT ANALYSIS OF THE SAME STUDY

>1 hr 30 mins more “Good On” time# per dose||

compared with IR CD/LD

#“Good On” time is defined as “On” time without troublesome dyskinesia.

||This was a post hoc analysis of the study; P<0.0001 vs IR CD/LD.

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MAIN MEASUREMENT

30 mins more “Good On” time† with less frequent dosing

In our main clinical study, people who took CREXONT an average of 3 times a day achieved 30 minutes more “Good On” time per day than those taking IR CD/LD an average of 5 times a day

“Good On” time is defined as “On” time without troublesome dyskinesia. Change in “Good On” time was measured by comparing values at the end of study to baseline; P=0.019 vs IR CD/LD.

This was the average dose frequency during the double-blind maintenance period.

In our main clinical study, people who took CREXONT an average of 3 times a day achieved 30 minutes more “Good On” time per day than those taking IR CD/LD an average of 5 times a day
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SECONDARY MEASUREMENT

30 mins less “Off” time per day§¶

People who took CREXONT had 30 minutes less “Off” time per day compared with those who took IR CD/LD

§This was a secondary endpoint of the study.

Study end=Week 20 or early termination; P=0.0252 vs IR CD/LD.

People who took CREXONT had 30 minutes less “Off” time per day compared with those who took IR CD/LD

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A DIFFERENT ANALYSIS OF THE SAME STUDY

>1 hr 30 mins more “Good On” time# per dose||

In a different analysis of our main clinical study of a dose-to-dose comparison, people took CREXONT fewer times per day and experienced over an hour and a half more “Good On” time per dose than people taking IR CD/LD

#“Good On” time is defined as “On” time without troublesome dyskinesia.

||This was a post hoc analysis of the study; P<0.0001 vs IR CD/LD.

In a different analysis of our main clinical study of a dose-to-dose comparison, people took CREXONT fewer times per day and experienced over an hour and a half more “Good On” time per dose than people taking IR CD/LD

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SAFETY

The most common side effects (incidence ≥3% and greater than IR CD/LD) were nausea and anxiety

See the latest results from an ongoing CREXONT study

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