A Research Study Investigating Semaglutide in People With Early Alzheimer's Disease (EVOKE)

Sponsor
Novo Nordisk A/S (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04777396
Collaborator
(none)
1,840
333
2
59.3
5.5
0.1

Study Details

Study Description

Brief Summary

This study is done to find out whether the medicine, semaglutide, has a positive effect on early Alzheimer's disease.

Participants will either get semaglutide or placebo (a "dummy" medicine which does not contain any study medicine) - which treatment participants get is decided by an equal chance.

The study will last for up to 173 weeks (about 3 years and 4 months). Participants will have 17 clinic visits and 1 phone call with the study doctor. The study includes various tests and scans. At 10 of the clinic visits participants will have blood samples taken.

Participants must have a study partner, who is willing to take part in the study.

Women cannot take part if pregnant, breastfeeding or plan to become pregnant during the study period.

A cerebrospinal fluid (CSF) sub-study will be performed as a part of the study. The sub-study will be performed on a selection of sites based on their experience with CSF sampling and willingness to participate in this sub-study. The endpoints related to this sub-study are exploratory only.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1840 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
Sponsor staff involved in the clinical trial is masked according to company standard procedures.
Primary Purpose:
Treatment
Official Title:
A Randomised Double-blind Placebo-controlled Clinical Trial Investigating the Effect and Safety of Oral Semaglutide in Subjects With Early Alzheimer´s Disease (EVOKE)
Actual Study Start Date :
May 18, 2021
Anticipated Primary Completion Date :
Aug 9, 2024
Anticipated Study Completion Date :
Apr 26, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Oral Semaglutide

Participants are given oral semaglutide once daily

Drug: Semagludtide
Oral semaglutide once-daily, dose gradually increased to 14 mg. The study will last for up to 173 weeks

Placebo Comparator: Placebo (semagludtide)

Participants are given oral placebo once daily

Drug: Placebo (semaglutide)
Oral placebo (semaglutide) once-daily, The study will last for up to 173 weeks

Outcome Measures

Primary Outcome Measures

  1. Change in the Clinical Dementia Rating - Sum of Boxes (CDR-SB) score [From baseline (week 0) to week 104]

    Score on scale (0 to 18) Measures the impact of cognitive decline on daily function using the following six domains commonly affected in Alzheimer's disease: Cognitive domains: memory, orientation, and judgement and problem solving Function domains: community affairs, home and hobbies, and personal care Based on clinical information obtained from the subject and informant, an individual box score ranging from 0 to 3 is determined that represents "none" to "severe" impairment for each of the six domains. The CDR-Sum of Boxes (CDR-SB) score will be derived by adding the individual scores of the six domains at a given time point. The total CDR-SB score ranges from 0 to 18 with higher scores representing greater impairment.

Secondary Outcome Measures

  1. Change in the Alzheimer's Disease Cooperative Study Activities of Daily Living Scale for MCI (ADCS-ADL-MCI) [From baseline (week 0) to week 104]

    Score on scale (0 to 53) An interview-based assessment of information provided by the study partner (informant). The total scores based on 18 items on the scale range from 0 to 53 with lower scores representing greater impairment.

  2. Time to progression to dementia (CDR global greater than or equal to 1.0) among subjects with MCI (CDR global equal to 0.5) at baseline [From baseline (week 0) to week 104]

    Week(s)

  3. Change in the Alzheimer's Disease Composite Score (ADCOMS) [From baseline (week 0) to week 104]

    Score on scale (0 to 1.97) The ADCOMS is a composite clinical outcome comprising 4 items from the ADAS-Cog-13, 2 items from the MMSE and all 6 items from the CDR-SB.32 The total scores on the scale range from 0 to 1.97 with higher scores indicating greater impairment.

  4. Change in the Mini-Mental State Examination (MMSE) score [From baseline (week 0) to week 104]

    Score on scale (0 to 30) The MMSE measures orientation, attention, memory, language and visuo-spatial function. The total scores on the scale range from 0 to 30 with lower scores indicating greater impairment.

  5. Change in the 10-item Neuropsychiatric Inventory (NPI) score [From baseline (week 0) to week 104]

    Score on scale (0 to 120) The 10-item scale assesses symptoms including delusions, hallucinations, agitation/aggression, dysphoria, anxiety, euphoria, apathy, disinhibition, irritability/lability and aberrant motor activity. For each domain the frequency (4-point scale) and severity (3-point scale) of symptoms is reported. The score for each domain is calculated by multiplying the frequency and severity score. The total 10-item NPI score is 0 to 120 with higher scores indicating a greater symptomatology.

  6. Time to progression in disease stage based on global CDR score [From baseline (week 0) to week 104]

    Week(s)

  7. Number of treatment emergent adverse events (TEAEs) [From baseline (week 0) to week 104]

    Number of events

  8. Change in high sensitivity C-reactive protein level [From baseline (week 0) to week 104]

    Ratio

  9. Time to first occurrence of major adverse cardiovascular event (MACE) comprising non-fatal myocardial infarction, non-fatal stroke and all-cause death [From baseline (week 0) to week 104]

    Week(s)

  10. Time to first occurrence of stroke [From baseline (week 0) to week 104]

    Week(s

  11. Change in the EQ-5D-5L proxy score [From baseline (week 0) to week 104]

    Score The EQ-5D-5L descriptive system comprises mobility, self-care, usual activities, pain/discomfort and anxiety/depression with five response levels each (no problems, slight problems, moderate problems, severe problems, unable to /extreme problems). The EQ-5D-5L proxy version 1 (the study partner is asked to rate how he/she [the proxy] would rate the subject´s health) will be used in this trial.

  12. Extension phase: Change in the CDR-SB score [From baseline (week 0) to week 156]

    Score on scale (0 to 18) Measures the impact of cognitive decline on daily function using the following six domains commonly affected in Alzheimer's disease: Cognitive domains: memory, orientation, and judgement and problem solving Function domains: community affairs, home and hobbies, and personal care Based on clinical information obtained from the subject and informant, an individual box score ranging from 0 to 3 is determined that represents "none" to "severe" impairment for each of the six domains. The CDR-Sum of Boxes (CDR-SB) score will be derived by adding the individual scores of the six domains at a given time point. The total CDR-SB score ranges from 0 to 18 with higher scores representing greater impairment.

  13. Change in the ADCS-ADL-MCI (Alzheimer's Disease Cooperative Study-Activities of Daily Living Inventory-Mild Cognitive Impairment ) score [From baseline (week 0) to week 156]

    Score on scale (0 to 53) An interview-based assessment of information provided by the study partner (informant). The total scores based on 18 items on the scale range from 0 to 53 with lower scores representing greater impairment.

  14. Time to progression to dementia (CDR global greater than or equal to 1.0) among subjects with MCI (CDR global equal to 0.5) at baseline [From baseline (week 0) to week 156]

    Week(s)

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male or female, aged 55-85 years (both inclusive) at the time of signing informed consent.

  • MCI (mild cognitive impairment) or mild dementia of the Alzheimer's type according to the NIA-AA (National Institute of Aging-Alzheimer's Association) 2018 criteria.

  • CDR (Clinical Dementia Rating) global score of 0.5 and CDR of 0.5 or more in at least one of the three instrumental activities of daily living categories (personal care, home & hobbies, community affairs) Or CDR global score of 1.0

  • RBANS (Repeatable Battery for the Assessment of Neuropsychological Status) delayed memory index score of below or equal to 85

  • MMSE (Mini-Mental State Examination) greater than or equal to 22

  • Amyloid positivity established with either amyloid PET (positron emission tomography), CSF (cerebrospinal fluid) Aβ1-42 or CSF Aβ1-42/Aβ1-40 .

  • If receiving an approved Alzheimer's disease treatment (such as acetylcholinesterase inhibitors, memantine or aducanumab) the dose must have been stable for at least 3 months prior to screening and should not be changed during the trial unless medically necessary.

Exclusion Criteria:
  • Brain MRI (or CT) scan suggestive of clinically significant structural CNS disease confirmed by central read (e.g. cerebral large-vessel disease [large vessel (cortical) infarcts greater than 10 mm in diameter], prior macro-haemorrhage [greater than 1 cm^3], cerebral vascular malformations, cortical hemosiderosis, intracranial aneurism(s), intracranial tumours, changes suggestive of normal pressure hydrocephalus).

  • Brain MRI (magnetic resonance imaging) (or CT) scan suggestive of significant small vessel pathology confirmed by central read and defined as greater than1 lacunar infarct and/or ARWMC (age-related white matter changes) greater than 2, (WM (white matter) greater than 20 mm) in the deep white matter and periventricular regions.

  • Brain MRI (or CT) scan suggestive of strategic infarcts defined as bilateral thalamic lacunar infarcts and singular paramedian thalamic infarcts confirmed by central read.

  • Evidence of a relevant neurological disorder other than MCI or mild dementia of the Alzheimer's type at screening, including but not limited to Parkinson's disease, Lewy body disease, frontotemporal dementia of any type, Huntington's disease, amyotrophic lateral sclerosis, multiple sclerosis, systemic lupus erythematosus, progressive supranuclear palsy, neurosyphilis, HIV (human immunodeficiency virus), learning disability, intellectual disability, hypoxic cerebral damage, or significant head trauma with loss of consciousness that led to persistent cognitive deficits

  • Evidence of a clinically relevant or unstable psychiatric disorder, based on Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria, including schizophrenia or other psychotic disorder, or bipolar disorder. A subject with a history of major depression who has not had an episode in the last 24 months before the day of screening and is considered in remission or whose depression is controlled with treatment can be included in the trial per investigator's judgement.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Novo Nordisk Investigational Site Phoenix Arizona United States 85006
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3 Novo Nordisk Investigational Site Tucson Arizona United States 85710
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8 Novo Nordisk Investigational Site Panorama City California United States 91402
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17 Novo Nordisk Investigational Site Atlantis Florida United States 33462
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146 Novo Nordisk Investigational Site Ulm Germany 89081
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148 Novo Nordisk Investigational Site Athens Greece GR-11521
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154 Novo Nordisk Investigational Site Budapest Hungary 1033
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161 Novo Nordisk Investigational Site Cork Ireland T12 WE28
162 Novo Nordisk Investigational Site Dublin Ireland D04 T6F4
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169 Novo Nordisk Investigational Site Ancona Italy 60126
170 Novo Nordisk Investigational Site Firenze Italy 50134
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179 Novo Nordisk Investigational Site Anjo-shi, Aichi Japan 446-8510
180 Novo Nordisk Investigational Site Arakawa-ku,Tokyo Japan 116-0014
181 Novo Nordisk Investigational Site Bunkyo-ku, Tokyo Japan 113-0034
182 Novo Nordisk Investigational Site Bunkyo-ku,Tokyo Japan 113-8519
183 Novo Nordisk Investigational Site Chib-shi, Chiba Japan 260-8656
184 Novo Nordisk Investigational Site Chofu-shi,Tokyo Japan 182-0036
185 Novo Nordisk Investigational Site Fujioka-Shi, Gunma Japan 375-0017
186 Novo Nordisk Investigational Site Hachioji-shi, Tokyo Japan 192-0071
187 Novo Nordisk Investigational Site Hamamatsu-shi, Shizuoka Japan 434-8511
188 Novo Nordisk Investigational Site Himeji-city, Hyogo Japan 670-0981
189 Novo Nordisk Investigational Site Himeji-shi, Hyogo Japan 671-1227
190 Novo Nordisk Investigational Site Himeji-shi, Hyogo Japan 672-8043
191 Novo Nordisk Investigational Site Hirakata-Shi,Osaka Japan 573-1121
192 Novo Nordisk Investigational Site Hiroshima-shi, Hiroshima Japan 732-0066
193 Novo Nordisk Investigational Site Hiroshima-shi, Hiroshima Japan 732-0822
194 Novo Nordisk Investigational Site Hofu-shi, Yamaguchi Japan 747-0802
195 Novo Nordisk Investigational Site Ina-shi, Nagano Japan 396-8555
196 Novo Nordisk Investigational Site Kawasaki-shi , Kanagawa Japan 214-0014
197 Novo Nordisk Investigational Site Kawasaki-shi, Kanagawa Japan 210-0852
198 Novo Nordisk Investigational Site Kawasaki-shi, Kanagawa Japan 213-8507
199 Novo Nordisk Investigational Site Kobe-shi, Hyogo Japan 650-0017
200 Novo Nordisk Investigational Site Kobe-shi, Hyogo Japan 650-0017
201 Novo Nordisk Investigational Site Kodaira-shi, Tokyo Japan 187-8551
202 Novo Nordisk Investigational Site Koriyama-shi, Fukushima Japan 963-8052
203 Novo Nordisk Investigational Site Kurashiki-shi, Okayama Japan 710-0813
204 Novo Nordisk Investigational Site Mitaka-shi,Tokyo Japan 181-0013
205 Novo Nordisk Investigational Site Nerima-ku, Tokyo Japan 179-0072
206 Novo Nordisk Investigational Site Niigata-shi, Niigata Japan 950-0983
207 Novo Nordisk Investigational Site Obu-shi, Aichi Japan 474-8511
208 Novo Nordisk Investigational Site Okayama-shi, Okayama Japan 703-8265
209 Novo Nordisk Investigational Site Shimotsuke-shi, Tochigi Japan
210 Novo Nordisk Investigational Site Shinjuku-ku, Tokyo Japan 160-0017
211 Novo Nordisk Investigational Site Shinjuku-ku, Tokyo Japan 160-8582
212 Novo Nordisk Investigational Site Takamatsu-shi, Kagawa Japan 760-8557
213 Novo Nordisk Investigational Site Takatsuki-Shi, Osaka Japan 569-1192
214 Novo Nordisk Investigational Site Tokorozawa-shi,Saitama Japan 359-1141
215 Novo Nordisk Investigational Site Tokushima-shi, Tokushima Japan 770-0852
216 Novo Nordisk Investigational Site Tokyo Japan 100-0005
217 Novo Nordisk Investigational Site Tokyo Japan 103-0028
218 Novo Nordisk Investigational Site Tokyo Japan 136-0075
219 Novo Nordisk Investigational Site Tokyo Japan 156-0041
220 Novo Nordisk Investigational Site Tokyo Japan 160-0023
221 Novo Nordisk Investigational Site Toride-shi, Ibaraki Japan 302-0004
222 Novo Nordisk Investigational Site Toyonaka-shi, Osaka Japan 560-0004
223 Novo Nordisk Investigational Site Wako-shi, Saitama Japan 351-0111
224 Novo Nordisk Investigational Site Yokohama-shi, Kanagawa Japan 223-0059
225 Novo Nordisk Investigational Site Busan Korea, Republic of 49201
226 Novo Nordisk Investigational Site Gyeonggi-do Korea, Republic of 13620
227 Novo Nordisk Investigational Site Incheon Korea, Republic of 21565
228 Novo Nordisk Investigational Site Incheon Korea, Republic of 22332
229 Novo Nordisk Investigational Site Seoul Korea, Republic of 04763
230 Novo Nordisk Investigational Site Seoul Korea, Republic of 05030
231 Novo Nordisk Investigational Site Seoul Korea, Republic of 05505
232 Novo Nordisk Investigational Site Seoul Korea, Republic of 06351
233 Novo Nordisk Investigational Site Saltillo Coahuila Mexico 25000
234 Novo Nordisk Investigational Site Guadalajara Jalisco Mexico 25000
235 Novo Nordisk Investigational Site Monterrey Nuevo León Mexico 64460
236 Novo Nordisk Investigational Site Monterrey Nuevo León Mexico 64620
237 Novo Nordisk Investigational Site Monterrey Nuevo León Mexico 64710
238 Novo Nordisk Investigational Site Culiacan Sinaloa Mexico 80020
239 Novo Nordisk Investigational Site Breda Netherlands 4818 CK
240 Novo Nordisk Investigational Site Den Bosch Netherlands 5223 LA
241 Novo Nordisk Investigational Site Haarlem Netherlands 2035 RC
242 Novo Nordisk Investigational Site Nijmegen Netherlands 6525 GA
243 Novo Nordisk Investigational Site Lørenskog Norway 1478
244 Novo Nordisk Investigational Site Oslo Norway 0450
245 Novo Nordisk Investigational Site Bydgoszcz Poland 85-163
246 Novo Nordisk Investigational Site Kielce Poland 25-411
247 Novo Nordisk Investigational Site Kraków Poland 30-688
248 Novo Nordisk Investigational Site Kraków Poland 31-505
249 Novo Nordisk Investigational Site Lublin Poland 20-818
250 Novo Nordisk Investigational Site Oswiecim Poland 32-600
251 Novo Nordisk Investigational Site Scinawa Poland 59-330
252 Novo Nordisk Investigational Site Sopot Poland 81-855
253 Novo Nordisk Investigational Site Warszawa Poland 01-684
254 Novo Nordisk Investigational Site Wroclaw Poland 53-659
255 Novo Nordisk Investigational Site Braga Portugal 4710-243
256 Novo Nordisk Investigational Site Coimbra Portugal 3000-561
257 Novo Nordisk Investigational Site Guimarães Portugal 4835-044
258 Novo Nordisk Investigational Site Matosinhos Portugal 4464-513
259 Novo Nordisk Investigational Site Porto Portugal 4099-001
260 Novo Nordisk Investigational Site Torres Vedras Portugal 2560-280
261 Novo Nordisk Investigational Site Timisoara Timis Romania 300766
262 Novo Nordisk Investigational Site Bucharest Romania 011025
263 Novo Nordisk Investigational Site Constanta Romania 900123
264 Novo Nordisk Investigational Site Constanta Romania 900591
265 Novo Nordisk Investigational Site Iasi Romania 700004
266 Novo Nordisk Investigational Site Sibiu Romania 550052
267 Novo Nordisk Investigational Site Timisoara Romania 300416
268 Novo Nordisk Investigational Site Ekaterinburg Russian Federation 620030
269 Novo Nordisk Investigational Site Kazan Russian Federation 420101
270 Novo Nordisk Investigational Site Kemerovo Russian Federation 650066
271 Novo Nordisk Investigational Site Krasnoyarsk Russian Federation 660037
272 Novo Nordisk Investigational Site Moscow Russian Federation 115522
273 Novo Nordisk Investigational Site Moscow Russian Federation 119021
274 Novo Nordisk Investigational Site Moscow Russian Federation 129226
275 Novo Nordisk Investigational Site Saint Petersburg Russian Federation 191015
276 Novo Nordisk Investigational Site Saint Petersburg Russian Federation 194044
277 Novo Nordisk Investigational Site Saratov Russian Federation 410028
278 Novo Nordisk Investigational Site Tomsk Russian Federation 634009
279 Novo Nordisk Investigational Site Belgrade Serbia 11000
280 Novo Nordisk Investigational Site Novi Sad Serbia 21000
281 Novo Nordisk Investigational Site Bardejov Slovakia 085 01
282 Novo Nordisk Investigational Site Bratislava Slovakia 813 69
283 Novo Nordisk Investigational Site Kosice Slovakia 041 66
284 Novo Nordisk Investigational Site Vranov nad Toplou Slovakia 093 01
285 Novo Nordisk Investigational Site Ljubljana Slovenia SI-1000
286 Novo Nordisk Investigational Site Maribor Slovenia SI-2000
287 Novo Nordisk Investigational Site Nova Gorica Slovenia SI-5000
288 Novo Nordisk Investigational Site George Eastern Cape South Africa 6529
289 Novo Nordisk Investigational Site Bloemfontein Free State South Africa 9301
290 Novo Nordisk Investigational Site Johannesburg Gauteng South Africa 2196
291 Novo Nordisk Investigational Site Pretoria Gauteng South Africa 0042
292 Novo Nordisk Investigational Site Cape Town Western Cape South Africa 7405
293 Novo Nordisk Investigational Site Cape Town Western Cape South Africa 7550
294 Novo Nordisk Investigational Site Cape Town Western Cape South Africa 7560
295 Novo Nordisk Investigational Site Barcelona Spain 08025
296 Novo Nordisk Investigational Site Barcelona Spain 08028
297 Novo Nordisk Investigational Site Donostia Spain 20009
298 Novo Nordisk Investigational Site Madrid Spain 28034
299 Novo Nordisk Investigational Site Madrid Spain 28041
300 Novo Nordisk Investigational Site Pozuelo de Alarcon Spain 28223
301 Novo Nordisk Investigational Site Sant Cugat del Vallès Spain 08195
302 Novo Nordisk Investigational Site Santander Spain 39008
303 Novo Nordisk Investigational Site Valencia Spain 46017
304 Novo Nordisk Investigational Site Malmö Sweden 205 02
305 Novo Nordisk Investigational Site Umeå Sweden 901 85
306 Novo Nordisk Investigational Site Biel-Bienne Switzerland 2501
307 Novo Nordisk Investigational Site Genève Switzerland 1205
308 Novo Nordisk Investigational Site Lausanne Switzerland 1011
309 Novo Nordisk Investigational Site St. Gallen Switzerland 9007
310 Novo Nordisk Investigational Site Eskisehir Turkey 26040
311 Novo Nordisk Investigational Site Istanbul Turkey 34093
312 Novo Nordisk Investigational Site Istanbul Turkey 34093
313 Novo Nordisk Investigational Site Izmir Turkey 35575
314 Novo Nordisk Investigational Site Samsun Turkey 55200
315 Novo Nordisk Investigational Site Kharkiv Ukraine 61091
316 Novo Nordisk Investigational Site Kyiv Ukraine 04114
317 Novo Nordisk Investigational Site Odesa Ukraine 65031
318 Novo Nordisk Investigational Site Vinnytsia Ukraine 21050
319 Novo Nordisk Investigational Site Aberdeen United Kingdom AB25 2ZH
320 Novo Nordisk Investigational Site Bath United Kingdom BA1 3NG
321 Novo Nordisk Investigational Site Crowborough United Kingdom TN6 1NY
322 Novo Nordisk Investigational Site Dundee United Kingdom DD1 9SY
323 Novo Nordisk Investigational Site Edinburgh United Kingdom EH4 2XU
324 Novo Nordisk Investigational Site Gloucestershire United Kingdom GL53 9DZ
325 Novo Nordisk Investigational Site London United Kingdom EC2Y 8EA
326 Novo Nordisk Investigational Site London United Kingdom SW17 0RE
327 Novo Nordisk Investigational Site London United Kingdom W12 0NN
328 Novo Nordisk Investigational Site Manchester United Kingdom M13 9WL
329 Novo Nordisk Investigational Site Motherwell United Kingdom ML1 4UF
330 Novo Nordisk Investigational Site Newcastle Upon Tyne United Kingdom NE4 5PL
331 Novo Nordisk Investigational Site Oxford United Kingdom OX3 7JX
332 Novo Nordisk Investigational Site Southampton United Kingdom SO30 3JB
333 Novo Nordisk Investigational Site Swindon United Kingdom SN3 6BW

Sponsors and Collaborators

  • Novo Nordisk A/S

Investigators

  • Study Director: Clinical Transparency (dept. 1452), Novo Nordisk A/S

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Novo Nordisk A/S
ClinicalTrials.gov Identifier:
NCT04777396
Other Study ID Numbers:
  • NN6535-4730
  • U1111-1259-2929
  • 2020-004848-29
First Posted:
Mar 2, 2021
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2022