CompletedPhase 2 / PHASE3

Study to Evaluate the Safety and Efficacy of Davunetide for the Treatment of Progressive Supranuclear Palsy

A Phase 2/3, Randomized, Double-Blind, Placebo-Controlled, Study to Evaluate the Safety and Efficacy of Davunetide for the Treatment of Progressive Supranuclear Palsy

Lead sponsor

Allon Therapeutics

Asset

Davunetide

Listed sites

Recruiting sites

Enrollment

313

actual

Study population

Frontotemporal dementia

Key I/E criteria

•MMSE ≥15•Study partner/caregiver required•MRI contraindications excluded

Primary endpoints

•Efficacy•Safety

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

Org study IDAL-108-231

NCT IDNCT01110720

Timeline

Milestones

Study first posted2010-04-27estimated

Study start2010-10 (month precision)

Primary completion2012-11actual (month precision)

Study completion2012-12actual (month precision)

Last update posted2013-01-17estimated

Assets

Drug assets

Davunetide

Study populations

Who this study enrolls

Frontotemporal dementia

Eligibility

Who can enroll

Minimum age41 Years

Maximum age85 Years

SexAll

Healthy volunteersNot accepted

Inclusion criteria

•Probable or possible PSP defined as:

-at least a 12-month history of postural instability or falls during the first 3 years that symptoms are present; and

-at screening, a decreased downward saccade velocity defined as observable eye movement (deviation from the "main sequence" linear relationship between saccade amplitude and saccade velocity) or, supranuclear ophthalmoplegia defined as 50% reduction in upward gaze or 30% reduction in downward gaze; and

-age at symptom onset of 40 to 85 years by history; and

-an akinetic-rigid syndrome with prominent axial rigidity.

•Aged 41 to 85 years at the time of screening.

•Judged by investigator to be able to comply with neuropsychological evaluation at baseline and throughout the study.

•Must have reliable caregiver accompany subject to all study visits. Caregiver must read, understand, and speak local language fluently to ensure comprehension of informed consent form and informant-based assessments of subject. Caregiver must also have frequent contact with subject (at least 3 hours per week at one time or at different times) and be willing to monitor study medication compliance and the subject's health and concomitant medications throughout the study.

•Modified Hachinski score ≤ 3 (Appendix 7). This modified Hachinski will not include the focal neurological signs, symptoms or pseudobulbar affect questions, given the prominence of all 3 in PSP.

•Score ≥ 15 on the mini-mental state examination (MMSE) at screening (Visit 1).

•Written informed consent provided by subject (or legally-appointed representative, as appropriate) and caregiver (if not the legally-appointed representative) who are both fluent local language speakers.

•Subject resides outside a skilled nursing facility or dementia care facility at the time of screening, and admission to such a facility is not planned. Residence in an assisted living facility is allowed.

•If the subject is receiving levodopa/carbidopa, levodopa/benserazide, a dopamine agonist, catechol-o-methyltransferase (COMT) inhibitor, or other Parkinson's medication,with teh exception of Azilect(rasagiline), the dose must have been stable for at least 60 days prior to the screening visit (Visit 1) and must remain stable for the duration of the study. No such medication can be initiated during the study. Subjects receiving rasagiline or CoQ10 must be on a stable dose for at least 90 days prior to the screening visit.

•Able to tolerate the MRI scan during screening with either no sedation or low dose lorazepam.

•Able to ambulate independently or with assistance defined as the ability to take at least 5 steps with a walker (guarding is allowed provided there is no contact) or the ability to take at least 5 steps with the assistance of another person who can only have contact with one upper extremity.

•Presence of symptoms for less than 5 years or the presence of symptoms for more than 5 years with a PSPRS baseline score ≥ 40.

•Stable on all other chronic medications for at least 30 days prior to the screening visit (Visit 1)

Exclusion criteria

•Insufficient fluency in local language to complete neuropsychological and functional assessments.

•A diagnosis of Amyotrophic Lateral Sclerosis or other motor neuron disease.

•Any of the following:

-Abrupt onset of symptoms defined in inclusion criteria 1 associated with ictal events,

-Head trauma related to onset of symptoms defined in inclusion criteria 1,

-Severe amnesia within 6 months of the symptoms defined in inclusion criteria 1,

-Cerebellar ataxia,

-Choreoathetosis,

-Early, symptomatic autonomic dysfunction; or

-Tremor while at rest.

•Presence of other significant neurological or psychiatric disorders including (but not limited to) Alzheimer's disease; dementia with Lewy bodies; prion disease; Parkinson's disease (which has not subsequently been revised to PSP); any psychotic disorder; severe bipolar or unipolar depression; seizure disorder; tumor or other space-occupying lesion; or history of stroke or head injury with loss of consciousness for at least 15 minutes within the past 20 years.

•Within 4 weeks of screening or during the course of the study, concurrent treatment with memantine; acetylcholinesterase inhibitors; antipsychotic agents (other than quetiapine) or mood stabilizers (e.g., valproate, lithium); or benzodiazepines (except as below).

-Low dose lorazepam (not more than 2 mg) may be used for sedation prior to MRI scans for those subjects requiring sedation. Neuropsychological testing may not be performed after lorazepam administration.

-Subjects who take short acting benzodiazepines (only temazepam or zolpidem are allowed) for sleep may continue to do so if they have been on a stable dose for 30 days prior to screening.

-Clonazepam may be used for treatment of dystonia or painful rigidity associated with PSP if the dose has been stable for 90 days prior to screening and is not expected to change during the course of the study.

•Treatment with lithium, methylene blue, tramiprosate, ketone bodies, latrepirdine, or any putative disease-modifying agent directed at tau within 90 days of screening.

•A history of alcohol or substance abuse within 1 year prior to screening and deemed to be clinically significant by the site investigator.

•Any malignancy (other than non-metastatic dermatological conditions) within 5 years of the screening visit (Visit 1) or current clinically significant hematological, endocrine, cardiovascular, renal, hepatic, gastrointestinal, or neurological disease. For the non-cancer conditions, if the condition has been stable for at least one year before the screening visit and is judged by the site investigator not to interfere with the subject's participation in the study, the subject may be included.

•Clinically significant laboratory abnormalities at screening, including creatinine ≥ 2.5 mg/dL, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 3 times the upper limit of the normal reference range, vitamin B12 below the laboratory normal reference range, or thyroid stimulating hormone TSH above laboratory normal reference range.

•The systolic blood pressure measurement is > 190 or < 85 mm Hg. The diastolic blood pressure measurement is > 105 or < 50 mm Hg at screening.

•Abnormal ECG tracing at screening and judged to be clinically significant by the site investigator.

•Treatment with any investigational drugs or device within 90 days of screening.

•Known history of serum or plasma progranulin level less than one standard deviation below the normal subject mean for the laboratory performing the assay.

•Known presence of known disease-associated mutation in TDP-43, PGRN, CHMPB2, or VCP genes or any other frontotemporal lobar degeneration (FTLD) causative genes not associated with underlying tau pathology (e.g., Chromosome 9 associated FTD).

•History of deep brain stimulator (DBS) surgery other than sham surgery for DBS clinical trial.

•History of early, prominent rapid eye movement (REM) sleep behavior disorder.

•Women who are pregnant or lactating and women of childbearing potential who are not using at least two different forms of medically recognized and highly effective methods of birth control, resulting in a low failure rate when used consistently and correctly such as implants, injectables, combined oral contraceptives, some IUDs, sexual abstinence or vasectomised partner.

•An employee or relative of an employee of the Sponsor, a clinical site, or Contract Research Organization participating in the study.

•Significant anatomical nasal abnormality (e.g., septal deviation obstructing airflow to at least one nostril or septal perforation) or history of nasal turbinate surgery.

•History of a clinically significant medical condition that would interfere with the subject's ability to comply with study instructions, would place the subject at increased risk, or might confound the interpretation of the study results.

•Contraindication to MRI examination for any reason (e.g., severe claustrophobia, ferromagnetic metal in body).

•Structural abnormality on MRI that precludes diagnosis of PSP, such as cortical infarct in brain region that might account for subject's symptoms.

•In subjects receiving anti-Parkinson's Disease medication at the time of screening, in the opinion of the investigator substantial worsening of motor signs or symptoms compared with normal functioning following overnight withdrawal of the anti-Parkinson medication.

•Known hypersensitivity to davunetide or any ingredient of the formulation.

Endpoints (5)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Function / daily living

Neuroimaging

Safety / tolerability / PK

Other clinical outcomes

Other (unclassified)

Function / daily living

1 endpoint

Primary/protocol endpoint

Efficacy, as measured by the change from baseline of the Schwab and England Activities of Daily Living Scale (SEADL) at 52 weeks

Time frame:52 weeks

change from baseline, improvement

Neuroimaging

1 endpoint

Secondary/protocol endpoint

Brain atrophy, as measured by change from baseline of ventricular volumes measured by volumetric brain MRI at 52 weeks.

Time frame:52 weeks

change from baseline, improvement

Safety / tolerability / PK

1 endpoint

Primary/protocol endpoint

Safety, as measured by reported AEs, electrocardiograms (ECG), nasal examinations and clinical laboratory measures

Time frame:52 weeks

descriptive

Other clinical outcomes

1 endpoint

Secondary/protocol endpoint

Efficacy, as measured by the Clinical Global Impression of Change (CGI-C) at 52 weeks

Time frame:52 weeks

descriptive

Other (unclassified)

1 endpoint

Primary/protocol endpoint/low confidence

Efficacy, as measured by change from baseline scores of the Progressive Supranuclear Palsy Rating Scale (PSPRS) at 52 weeks

Time frame:52 weeks

change from baseline, improvement

Publications (2)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2

Snapshot dateJuly 21, 2026

Endpoint classificationDelfa ADRD endpoint taxonomy

Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 21, 2026 snapshot.