Table 2.
Drug name | Mechanism of action | Disease stage | Dose and administration route | Sample size | Primary outcome | Results |
---|---|---|---|---|---|---|
Exenatide (47) | Antihyperglycemic; glucagon-like peptide 1 (GLP-1) receptor agonist | Moderate PD | 2 mg or placebo, subcutaneous injections | 62 | MDS-UPDRS, motor scores (part 3) in the practically defined off-medication state | Mild improvement in the intervention group in comparison to placebo difference of −3.5 points (−6.7 to −0.3; p = 0.0318) |
Nilotinib (48) | BCR-ABL inhibitor used for treatment of leukemia | Cohort 1—moderate to advanced PD Cohort 2—early/de novo PD |
150 or 300 mg; oral | 76 | Safety and Tolerability; MDS-UPDRS, motor scores part III | Drug was well-tolerated. MDS-UPDRS-part III was worse in the Nilotinib 300 mg group |
Pioglitazone (49) | Antihyperglycemic, inhibit the activation of microglia and astrocytes and production of pro-inflammatory cytokines and nitric oxide | Early PD diagnosed within 5 years | 15, 45 mg/day, or placebo; oral | 210 | Total UPDRS score | Negative results |
Transdermal Nicotine NIC-PD (NCT01560754) | Agonist of nicotine receptor, modulate dopaminergic function | Early PD up to 18 months of diagnosis | 7 or 14 mg nicotine titrated up to 28 mg, or placebo; transdermal | 160 | UPDRS score (parts 1 to 3) Parkinson's Disease Questionnaire−8 (PDQ-8) |
Unpublished |
Isradipine (50) STEADY-PD III |
Dihydropyridine calcium-channel blocker, used for hypertension | Early PD not requiring symptomatic treatment | 5 mg BID or placebo; oral | 336 | UPDRS score (parts 1 to 3) | Negative results |
Inosine (51) SURE-PD3 |
Urate precursor used for urate elevation | Early PD not requiring symptomatic treatment | Inosine to produce mild elevation of urate; inosine to produce moderate elevation; or placebo | 75 | Safety and Tolerability; Elevation of urate assessed serially in serum in cerebrospinal fluid | Negative results |
PDQ, Parkinson's Disease Questionnaire; UPDRS, Unified Parkinson Disease Rating Scale.