Simufilam (PTI-125), 100 mg, for Mild-to-moderate Alzheimer's Disease Patients

C

Cassava Sciences

Status and phase

Completed
Phase 2

Conditions

Alzheimer Disease

Treatments

Drug: Placebo
Drug: Simufilam 100 mg oral tablet

Study type

Interventional

Funder types

Industry
NIH

Identifiers

NCT04388254
PTI-125-04
R44AG065152 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

A two-year safety study of simufilam (PTI-125) 100 mg oral tablets twice daily for participants of the previous simufilam studies as wells as additional new mild-to-moderate Alzheimer's disease subjects for a total of 200 participants. All participants will receive simufilam 100 mg tablets twice daily for one year, followed by a 6-month randomized, double-blind period where subjects will either continue on active treatment or be switched to placebo. The study concludes with an additional 6-month open-label treatment period. Clinic visits are every month or month and a half in the first year, and every 3 months in the second year with an additional visit at Month 13. Cognition and neuropsychiatric symptoms are evaluated.

Full description

The objectives of this study are to build the safety database for simufilam (PTI-125) and to investigate its effects on biomarkers, cognition and neuropsychiatric symptoms during 12-month twice-daily administration in mild-to-moderate AD patients. Additional objectives are to assess differences in cognition and neuropsychiatric symptoms between active and placebo arms in the 6-month randomized period. All subjects will undergo lumbar puncture at screening for baseline testing of cerebrospinal fluid (CSF) total tau and Abeta42, and the first 50 subjects will also provide a CSF sample at Month 6 or Month 12 for evaluation of change from baseline in CSF biomarkers. CSF will not be required of subjects with prior CSF, PET or MRI evidence of Alzheimer's disease. Plasma biomarkers will be evaluated in all subjects. Safety will be assessed by blood tests, electrocardiograms, adverse event monitoring and, at Months 12 and 24, full physical examinations.

Enrollment

220 patients

Sex

All

Ages

50 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Informed consent form (ICF) signed by the subject or legally acceptable representative.
  2. Patient has a caregiver or legal representative responsible for administering the drug and recording the time.
  3. Ages ≥ 50 and ≤ 85 years
  4. Clinical diagnosis of dementia due to possible or probable AD consistent with criteria established by a workgroup of the National Institute on Aging and the Alzheimer's Disease Association.
  5. If female, postmenopausal for at least 1 year
  6. Patient living at home, senior residential setting, or an institutional setting without the need for continuous (i.e. 24-h) nursing care
  7. General health status acceptable for participation in the study
  8. Fluency (oral and written) in English or Spanish
  9. If receiving memantine, rivastigmine, galantamine or an AChEI, receiving a stable dose for at least 3 months (90 days) before screening. If receiving donepezil, receiving any dose lower than 23 mg once daily. Multiple medications are allowed.
  10. The patient is a non-smoker for at least 3 years.
  11. The patient or legal representative must agree to comply with the drawing of blood samples for the PK assessments, laboratory assessments and SavaDx.
  12. MMSE-2 score ≥ 16 and ≤ 26 at screening, OR if > 26, must have evidence of AD pathology such as a prior CSF total tau/Aβ42 ratio ≥ 0.28, an amyloid positive PET scan or hippocampal volume loss consistent with AD.

Exclusion criteria

  1. Anything that in the opinion of the Investigator would preclude participation in a 2-year study.
  2. BMI < 18.5
  3. Positive urine drug screen.
  4. Positive HIV, HCV or HbsAg screen.
  5. Suicidality on C-SSRS
  6. Exposure to an experimental drug other than simufilam, experimental biologic or experimental medical device within 3 months before screening
  7. A medical condition that would interfere with a lumbar puncture
  8. Residence in a skilled nursing facility and requiring 24 h care.
  9. Clinically significant laboratory test results
  10. Clinically significant untreated hypothyroidism (if treated, thyroid-stimulating hormone level and thyroid supplementation dose must be stable for at least 6 months before screening)
  11. Insufficiently controlled diabetes mellitus, including requiring insulin or metformin >1000 mg/day.
  12. Renal insufficiency (serum creatinine > ULN and clinically significant in the opinion of PI and/or Sponsor OR eGFR <60 ml/min/m2 as estimated by either the MDRD or CKD-EPI equation)
  13. Malignant tumor within 3 years before screening (except squamous and basal cell carcinoma or cervical carcinoma in situ or localized prostate cancer or localized stage 1 bladder cancer)
  14. History of ischemic colitis or ischemic enterocolitis
  15. Unstable medical condition that is clinically significant in the judgment of the investigator
  16. Alanine transaminase (ALT) or aspartate transaminase (AST) > ULN or total bilirubin > ULN and clinically significant in the opinion of PI and/or Sponsor.
  17. History of myocardial infarction or unstable angina within 6 months before screening
  18. History of more than 1 myocardial infarction within 5 years before screening
  19. Clinically significant cardiac arrhythmia (including atrial fibrillation), cardiomyopathy, or cardiac conduction defect (patients with a pacemaker are acceptable)
  20. Symptomatic hypotension, or uncontrolled hypertension
  21. Clinically significant abnormality on screening electrocardiogram (ECG), including but not necessarily limited to a confirmed QTc (Fridericia correction method) value ≥ 450 msec for males or ≥ 470 msec for females.
  22. Stroke within 18 months before screening, or history of a stroke concomitant with onset of dementia
  23. History of brain tumor or other clinically significant space-occupying lesion on CT or MRI
  24. Head trauma with clinically significant loss of consciousness within 12 months before screening or concurrent with the onset of dementia
  25. Onset of dementia secondary to cardiac arrest, surgery with general anesthesia, or resuscitation
  26. Specific degenerative CNS disease diagnosis other than AD (e.g., Huntington's disease, Creutzfeld-Jacob disease, Down's syndrome, Frontotemporal Dementia, Parkinson's disease)
  27. Wernicke's encephalopathy
  28. Active acute or chronic CNS infection
  29. Donepezil 23 mg or greater QD currently or within 3 months prior to randomization
  30. Discontinued AChEI < 30 days prior to randomization
  31. Antipsychotics; low doses are allowed only if given for sleep disturbances, agitation and/or aggression, and only if the subject has received a stable dose for at least 3 months before randomization
  32. Tricyclic antidepressants and monoamine oxidase inhibitors; all other antidepressants are allowed only if the subject has received a stable dose for at least 3 months before randomization
  33. Anxiolytics or sedative-hypnotics, including barbiturates (unless given in low doses for benign tremor); low doses of benzodiazepines and zolpidem are allowed only if given for insomnia/sleep disturbance, and only if the subject has received a stable dose for at least 3 months before randomization
  34. Immunosuppressants, including systemic corticosteroids, if taken in clinically immunosuppressive doses (Steroid use for allergy or other inflammation is permitted.)
  35. Antiepileptic medications if taken for control of seizures
  36. Chronic intake of opioid-containing analgesics
  37. Sedating H1 antihistamines
  38. Nicotine therapy (all dosage forms including a patch), varenicline (Chantix), or similar therapeutic agent within 30 days before screening
  39. Clinically significant illness within 30 days of enrollment
  40. History of significant neurological, hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, or metabolic disease
  41. Loss of a significant volume of blood (> 450 mL) within 4 weeks prior to the study
  42. COVID-19 infection within 3 months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

220 participants in 2 patient groups, including a placebo group

Simufilam 100 mg oral tablets throughout
Experimental group
Description:
Simufilam 100 mg oral tablets administered twice daily (BID) for the full 24 months (including the randomized period Month 12 to Month 18)
Treatment:
Drug: Simufilam 100 mg oral tablet
Simufilam 100 mg oral tablets / Placebo / Simufilam 100 mg oral tablets
Placebo Comparator group
Description:
This placebo arm is only for Month 12 to Month 18. Day 1 to Month 12, as well as Month 18 to Month 24 are open-label treatment periods of simufilam 100 mg b.i.d. for all subjects.
Treatment:
Drug: Simufilam 100 mg oral tablet
Drug: Placebo

Trial contacts and locations

17

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Data sourced from clinicaltrials.gov

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