Efficacy in monotherapy*

Powerful efficacy in monotherapy* with significant improvements in patients' daily activities1,2

Efficacy measure: Change from baseline to week 26 in MDS-UPDRS Part II score

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JUVMO™ was studied in the TEMPO-1 Trial. See MDS-UPDRS Part II score when used as monotherapy.

TEMPO-1: Phase 3, randomized, double-blind, placebo-controlled, fixed-dose, 27-week trial in 529 patients with early PD.1,2

*In the TEMPO-1 clinical trial, 27% of JUVMO patients (n=95/354) were taking MAO-B inhibitors at baseline.2

Powerful efficacy in monotherapy* with significant improvements in patients' daily activities1,3

Efficacy measure: Change from baseline to week 26 in MDS-UPDRS Part II score

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JUVMO™ was studied in the TEMPO-2 Trial. See MDS-UPDRS Part II score when used as monotherapy.

TEMPO-2: Phase 3, randomized, double-blind, placebo-controlled, flexible-dose, 27-week trial in 304 patients with early PD.1,3

*In the TEMPO-2 clinical trial, 30% of JUVMO patients (n=46/151) were taking MAO-B inhibitors at baseline.3

Change in MDS-UPDRS Part III score from baseline to week 264

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JUVMO™ was studied in the TEMPO-1 Trial. See MDS-UPDRS Part III score when used in monotherapy.

TEMPO-1: Phase 3, randomized, double-blind, placebo-controlled, fixed-dose, 27-week trial in 529 patients with early PD.1,2

Data Limitations: Data are prespecified endpoints not adjusted for multiplicity; no conclusions of statistical significance can be made.

Change in MDS-UPDRS Part III score from baseline to week 264

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JUVMO™ was studied in the TEMPO-2 Trial. See MDS-UPDRS Part III score when used in monotherapy.

TEMPO-2: Phase 3, randomized, double-blind, placebo-controlled, flexible-dose, 27-week trial in 304 patients with early PD.1,3

Data Limitations: Data are prespecified endpoints not adjusted for multiplicity; no conclusions of statistical significance can be made.

TEMPO-1 (without oral levodopa)

Patient-reported improvements in Parkinson's symptoms at week 26 (PGIC scale)2,5*

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See the percentage of patients taking JUVMO™ who reported improvements in their Parkinson's symptoms.

Key Secondary Endpoint: About 45% of patients taking JUVMO 5 mg or 15 mg reported that PD symptoms had much improved or very much improved vs 12.2% of patients taking placebo.2

TEMPO-1: Phase 3, randomized, double-blind, placebo-controlled, fixed-dose, 27-week trial in 529 patients with early PD.1,2

PGIC Limitations: PGIC scales have the potential to introduce recall bias and error since they require the subject to compare their current status to their status from an earlier timepoint.

Post Hoc Limitations: Data derived from a post hoc analysis are not adjusted for multiplicity; no conclusions of statistical significance can be drawn due to the exploratory nature of the analysis.

*Based on a 7-point response scale. The participant's response to the question, "Compared to your condition at the beginning of treatment, how much has your condition changed?" was assessed. Scores ranged from 1 to 7 on a scale of 1 (very much improved) to 7 (very much worse). Higher values represent a worse outcome.6

Man riding his bike.

AI-generated depiction. Not a real patient.

Review safety data from the JUVMO studies

BL=baseline; LS=least squares; MAO-B=monoamine oxidase-B; MDS-UPDRS=Movement Disorder Society-Unified Parkinson’s Disease Rating Scale; OLE=open-label extension; PD=Parkinson's disease; PGIC=Patient Global Impression of Change.