NCT05065216ClinicalTrials.gov

Treatment of Acute Ischemic Stroke (ReMEDy2 Trial)

Phase 2/3 Adaptive Design, Randomized Double-blind Placebo-controlled Study to Evaluate the Safety and Efficacy of DM199 for the Treatment of Acute Ischemic Stroke (ReMEDy2 Trial)

In reclutamentoAccetta partecipanti ora, secondo la scheda del registro.

Contatta questo studio

In breve

Fase 2 / Fase 3728 partecipanti ricercati86 centri10 paesi

Categorie

Cardiovascolare71%Neurologia29%

Registrato in 1 registro

ClinicalTrials.govNCT05065216Apri questa scheda su ClinicalTrials.govSincronizzato 5 giorni fa

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How this study is set up

The points below are drawn from the public registry record for this study. Each one cites the field or sentence it came from. A dash (—) means the record does not state something — not that it is missing or wrong. Many well-run studies, especially small ones, leave some of these blank.

Present: Registered before enrolment beganFirst posted 2021-10-04; recorded start 2021-11-07
Present: Has a defined primary outcomeA primary outcome measure is listed in the record
Present: The primary outcome states a time frameThe primary outcome measure records a time frame
Present: Participants are randomly assignedAllocation is recorded as randomised
Present: Has a comparison groupThe record lists a placebo or comparator arm, or more than one study arm
Present: Uses blinding (masking)A masking level is recorded in the record
Not stated: An ethics committee is not stated in the registry recordThis registry's ingested record has no ethics-committee field
Not stated: Regulatory oversight (such as an IND or IDE) is not stated in the registry recordThis registry's ingested record has no regulatory-authorisation field
Not stated: A data monitoring committee is not stated in the registry recordThis registry's ingested record has no data-monitoring-committee fieldA data monitoring committee is not required for many smaller studies, and its absence here is not unusual.
Present: No cost to participants is mentioned in the recordChecked the summary, description and eligibility text; no cost-to-participant phrase found
Present: Sponsor has 2 other studies in this databaseCounted from the lead sponsor named in the record (DiaMedica Therapeutics Inc)
Not stated: No posted results from this sponsor are in this database yetBased on the sponsor’s studies in this database

The record lists 3 conditions.
Lead sponsor type recorded as: industry.
Intervention regulatory context: investigational, within a phased regulatory pathway.

These are facts from the public registry record, not a judgement about the study. Discuss any trial with your own doctor before taking part.

What these facts mean, and what to ask · ruleset v1

Trial stature

Three independent measures of this study, described from its registry record — not a recommendation about it. A rigorous study by investigators nobody has heard of is better evidence than a weak study led by a famous one. How these are scored.

Methodological rigourDEFINITIVE

A definitive-grade design for a phase 3 study, judged from its ClinicalTrials.gov record.

How this score is built

Randomised allocation20/20
Participants are randomly allocated between arms
Blinding13/20
Double-blind
Control arm13/15
Placebo / sham control arm
Primary-outcome specificity10/10
Named primary outcome with a defined time frame
Endpoint type7/10
Clinical-event endpoint
Multi-centre8/8
Multi-centre: 66 sites
Data monitoring committee7/7
A data monitoring committee is in place
Prospective registration5/5
Registered before the study start date
Protocol / SAP posted0/5
No protocol or SAP posted to the registry

ScaleMEDIUM

A medium-sized study, international in scope: 728 participants (target), run at 86 sites, across 10 countries.

How this score is built

Enrolment28/40
728 participants (target)
Site count21/25
66 sites
Country count12/15
9 countries
Planned duration10/10
Planned over about 62 months
Sponsor scale1/10
DiaMedica Therapeutics Inc has led 3 trials in our corpus

Investigator standingUNKNOWN

We have no verifiable track record for the investigator named on this trial. That is common for early-career investigators and for records held outside ClinicalTrials.gov — it is not a negative signal.

How this score is built

Investigator standing0/100
No investigator recorded in the registry for this trial

These describe the registry record only, and today we hold ClinicalTrials.gov data. Absent fields lower a score, and absence often reflects registration practice rather than study quality. A high-stature trial is not necessarily safer or a better choice for you — enrolling in a large definitive trial can mean a higher chance of receiving placebo, while a small early-phase study may be the only route to a new therapy.

Sintesi

This is a Phase 2/3 study evaluating the safety and efficacy of DM199 (rinvecalinase alfa) in treating participants with moderate stroke severity, who present within 24 hours of Acute Ischemic Stroke (AIS) onset due to small and medium vessel occlusions. This study focuses on participants with limited treatment options. Participants who have or will receive mechanical thrombectomy (MT) are not eligible for participation. Additionally, participants who have received fibrinolytics are excluded unless they experience a persistent neurological deficit of moderate severity six or more hours after fibrinolytic treatment. Participants considered for this trial should not be denied the use of standard of care (SoC) AIS therapies, such as fibrinolytics or MT, when appropriate. The double-blinded study will be randomized and placebo-controlled at up to approximately 100 sites.

This is a Phase 2/3 Adaptive Design, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of DM199 for the Treatment of Acute Ischemic Stroke (ReMEDy2 Trial). Participants with AIS will be randomized 1:1 to DM199 or placebo. DM199 will be administered as a single intravenous (IV) dose (0.5 μg/kg; not to exceed 50 μg) followed by subcutaneous (SC) doses at 2 hours (+10 hours) of the IV dose completion and then 2 times per week up to Day 21. The duration of each individual's participation in the study will be approximately 90 days from the time of initial treatment to completion of all study activities. A formal interim analysis will be conducted after 200 participants complete their Day 90 assessment in Part A. The purposes of this interim analysis are to assess safety, allow early stopping of the study for futility, or continuing the study with a revised final sample up to a maximum of 728 participants.

Patologie

Acute Stroke
Ischemic Stroke
Stroke

Idoneità

Idoneità
Sesso	Tutti
Età	18 Years – 90 Years
Volontari sani	No

Idoneità come riportata nel registro

Inclusion Criteria: 1. Participant is between 18 and 90 years of age inclusive. 2. Participant weight is 40 kg to 166 kg inclusive. 3. Participant to be randomized and treatment initiated within 24 hours of last known normal/AIS stroke onset. 4. Participant has NIHSS ≥5 and ≤15 at approximately the time of randomization. This criterion also applies to participants who meet the following conditions: * The participant initially presents with an NIHSS score below 5 but clinically worsens, including cases of progressing stroke / stroke-in-evolution, resulting in a subsequent persistent NIHSS score of ≥5 and ≤15; and * Participant meets all other inclusion and exclusion criteria, including repeat brain imaging to rule out hemorrhagic transformation. 5. Participant had a pre-morbid mRS score of 0 to 1 (mRS score prior to AIS) as stated by participant or participant's representative. 6. If participant has received fibrinolytic treatment for AIS within 4.5 hours of last know normal/AIS stoke onset and at least 6 hours after completing fibrinolytic treatment, and the participant meets all of the following criteria: * Participant's initial NIHSS score prior to fibrinolytics was ≤15; and * At least six hours after fibrinolytics, the participant has NIHSS score of ≥5 and ≤15 with a persistent deficit; and * The participant's NIHSS score showed less than a 4-point improvement, or worsened, after receiving fibrinolytics; and * Participant meets all other inclusion and exclusion criteria including repeat brain imaging to rule out hemorrhagic transformation. 7. Participant and/or legally authorized representative is able to provide informed consent. 8. Participant is willing and able to comply with the study protocol, in the Investigator's judgment. Exclusion Criteria: 1. At screening, or with repeat imaging (see Inclusion 4 and 6), participant has imaging confirmed hemorrhage stroke. 2. Participant has image findings with symptomatic large vessel occlusion at one or more of the following locations: Intracranial carotid I/T/L or M1 segment MCA, vertebral or basilar artery (BA). 3. Participant has large core of established infarction defined as ASPECTS 0-5. 4. Participant has or will receive MT for their current AIS. 5. Participant has suspected or confirmed extracranial arterial dissection. 6. Participant has imaging findings and/or symptoms consistent with a brain stem or cerebellar stroke. Posterior cerebral artery strokes without any associated brain stem or cerebellar involvement are allowable. 7. Participant has any recorded SBP \<100 mmHg or MAP \<65 mmHg; MAP = DBP + \[1/3 (SBP - DBP)\] (measured with noninvasive BP cuff type monitor) after stroke symptom onset and prior to randomization. 8. Participant is currently prescribed angiotensin-converting enzyme inhibitor (ACEi) and is unable or unwilling to convert to another antihypertensive pharmacological treatment through Day 29 ±1 day (8 days after last treatment). 9. Participant is currently prescribed an ACEi, and the last dose of the ACE inhibitor medication is reported to have been taken \< 24 hours before start of IV study drug infusion as stated by participant or participant's representative. 10. Participant has a history of clinically significant allergic reactions such as angioedema or anaphylaxis requiring hospitalization. 11. Participant has a diagnosis or suspected diagnosis of hereditary angioedema (HAE) or is taking or prescribed medications commonly used as prophylaxis/treatment of HAE, such as C1-esterase inhibitors (Cinryze, Berinert, Ruconest, Haegarda), Danazol, kallikrein inhibitors (Ecallantide, Berotralstat, Lanadelumab), Bradykinin B2 Receptor Antagonists (Icatibant), or other medication designed to influence the kallikrein-kinin system. 12. Life expectancy estimated at ≤1 year prior to enrollment. 13. Participant has clinical evidence of an active infection at the time of enrollment requiring parenteral treatment or hospitalization to monitor or manage the infection. NOTE: Treatment of uncomplicated infections with oral antibiotics would not be an exclusion (for example, the treatment of uncomplicated urinary tract infections or sinus infections with oral antibiotics would not be exclusionary). 14. Participant has known alpha 1-antitrypsin deficiency (α1-antitrypsin deficiency). 15. Participant is pregnant or nursing. NOTE: Participants who agree to stop nursing may be considered for inclusion at the discretion of the Investigator. 16. Participants of child-bearing potential must agree to use medically acceptable contraceptive measures to prevent pregnancy. All participants of childbearing potential (defined as sexually mature participants who have had menses within the preceding 24 months and have not undergone permanent sterilization methods such as hysterectomy, bilateral oophorectomy, bilateral salpingectomy, etc.) must have a negative serum pregnancy test performed locally at screening. Participants of childbearing potential must agree not to attempt to become pregnant or undergo in vitro fertilization. If participating in sexual activity that could lead to pregnancy, participants must use 2 reliable methods (1 per partner is acceptable) of contraception simultaneously while receiving protocol-specified medication and during the study follow-up period. Participants participating in sexual activity must agree to use, or for their partner to use highly effective birth control methods (those with a failure rate of less than 1% per year when used consistently and correctly) until they have completed the study (after the Day 90 visit). Such methods include: * Combined (estrogen and progesterone containing) hormonal oral, intravaginal, or transdermal contraception associated with the inhibition of ovulation * Progesterone-only oral, injectable, or implantable hormonal contraception associated with the inhibition of ovulation * Intrauterine device (IUD) * Intrauterine hormone-releasing system (IUS) * Bilateral tubal occlusion * Vasectomized partner * Sexual abstinence Participants who are not of reproductive potential (who have been postmenopausal for more than 24 consecutive months or have undergone hysterectomy, bilateral oophorectomy, bilateral salpingectomy, etc.) are not required to use contraception. Participants are prohibited from sperm donation. NOTE: A negative serum pregnancy test will be documented during screening if a participant is of child-bearing potential. 17. Participant is currently participating in or has participated in a study using an investigational device or drug or received an investigational drug or investigational use of a licensed drug within 30 days prior to screening. 18. Participant does not have sufficient venous access for infusion of study treatment or blood sampling. 19. Participant is unable or unwilling to comply with protocol requirements, including assessments, tests, and follow-up visits. 20. Participant has any other medical condition which in the opinion of the Investigator will make participation medically unsafe or interfere with the study results.

Idoneità in frasi semplici

I criteri di questa scheda non sono ancora stati suddivisi in affermazioni distinte. Il testo del registro qui sopra è completo ed è la versione autorevole.

Disegno dello studio

Disegno dello studio
Tipo di studio	Interventistico
Fase	Fase 2 / Fase 3
Assegnazione	Randomizzata
Modello di intervento	PARALLEL
Finalità principale	TREATMENT
Mascheramento	DOUBLE (2)
Arruolamento	728 partecipanti ricercati

Sponsor e collaboratori

DiaMedica Therapeutics Inc Sponsor

Bracci e interventi

DM199EXPERIMENTAL
DM199 administered by a single intravenous (IV) dose followed by subcutaneous (SC) doses at 2 hours (+10 hours) of the IV dose completion and then 2 times per week up to Day 21.
Placebo for DM199 Solution for InjectionPLACEBO_COMPARATOR
Placebo administered by a single intravenous (IV) dose followed by subcutaneous (SC) doses at 2 hours (+10 hours) of the IV dose completion and then 2 times per week up to Day 21.

Interventi

Altro Placebo for DM199 Solution for Injection
Placebo administered by a single intravenous (IV) dose followed by subcutaneous (SC) doses at 2 hours (+10 hours) of the IV dose completion and then 2 times per week up to Day 21.
Farmaco Recombinant human tissue kallikrein
DM199 administered by a single intravenous (IV) dose followed by subcutaneous (SC) doses at 2 hours (+10 hours) of the IV dose completion and then 2 times per week up to Day 21

Esiti misurati

Esito primario
Stroke Recovery
Stroke recovery as defined by participants with excellent functional outcomes at Day 90 as assessed via the Modified Rankin Score (mRS \[dichotomized\]), mRS scores of 0 or 1 represent responders, scale range of 0-6. The mRS (Modified Rankin Scale) is a single-item, clinician-reported measure of functional disability in participants with AIS. Scores range in grade from 0 (no symptoms at all) to 6 (participant death).
Orizzonte temporale Day 90
Esito secondario
Effect on Disability
Assessment of effect on disability across the full spectrum of AIS by examining the distribution of mRS (shift) scores (scale range = 0 to 6) at Day 90. The mRS (Modified Rankin Scale) is a single-item, clinician-reported measure of functional disability in participants with AIS. Scores range in grade from 0 (no symptoms at all) to 6 (participant death).
Orizzonte temporale Day 90
Esito secondario
Independent Function
Proportion of participants achieving independent function (able to look after their own affairs without assistance) with or without minor disability at Day 90 assessed as mRS 0-2 (dichotomized) mRS scores of 0, 1 or 2 represent responders, scale range of 0-6. The mRS (Modified Rankin Scale) is a single-item, clinician-reported measure of functional disability in participants with AIS. Scores range in grade from 0 (no symptoms at all) to 6 (participant death).
Orizzonte temporale Day 90
Esito secondario
Mortality Rate
Mortality rate as defined by event rate (%) for mortality over 90 days.
Orizzonte temporale Day 90
Esito secondario
Neurological Outcome
Proportion of participants achieving an excellent neurological outcome defined by National Institute of Health Stroke Scale (NIHSS)= 0-1 (dichotomized) (NIHSS scores of 0 or 1, scale range 0 to 42) at Day 90. The National Institute of Health Stroke Scale (NIHSS) is a clinician-reported measure used to rate the severity of strokes, namely disability and recovery after acute stroke. The scale is comprised of 11 items with item scores ranging from 0 to 4. Total scores range from 0 to 42, with higher scores indicating increased severity.
Orizzonte temporale Day 90
Esito secondario
Functional Independence
Proportion of participants achieving an excellent functional independence in activities of daily living defined by Barthel Index score (dichotomized) greater than or equal to 5 (scale range 0 to 100) at Day 90. The Barthel Index (BI) is a 10-item scale assessing activities of daily living and functional disability. Each item is scored in increments of 5 points (0, 5, 10, or 15) and the individual items are summed to produce a total score between 0 and 100, with higher scores representing more optimal performance (100 = fully independent) and lower scores representing inferior performance (0 = totally dependent).
Orizzonte temporale Day 90
Esito secondario
AIS Recurrence
Recurrent AIS as defined by proportion of participants who experience a recurrent AIS by Day 90 as assessed by a new, persistent neurological deficit attributable to cerebrovascular ischemia. Imaging findings, if available, should support the diagnosis.
Orizzonte temporale Day 90

Date

Date
Data di inizio	7 novembre 2021 (effettiva)
Conclusione primaria	1 dicembre 2026 (stimata)
Conclusione	1 dicembre 2026 (stimata)
Prima pubblicazione	4 ottobre 2021 (effettiva)
Ultimo aggiornamento	14 settembre 2026
Risultati pubblicati	Non indicato nella scheda del registro
Stato verificato l'ultima volta	settembre 2026

«Effettiva» significa che l'evento è avvenuto. «Stimata» significa che lo sponsor lo prevede. Le due cose non sono equivalenti.

Centri

78 centri stanno reclutando

Belgium

Belgium
Struttura	Città	Stato o regione	Stato
Imeldaziekenhuis (Imelda Hospital)	Bonheiden	Belgium	In reclutamento
UZ Gent	Ghent	Belgium	In reclutamento
Jessa Ziekenhuis	Hasselt	Belgium	In reclutamento
AZ Groeninge	Kortrijk	Belgium	In reclutamento
CHC Montléga	Liège		In reclutamento
Clinique St Pierre	Ottignies	Belgium	In reclutamento

Canada

Canada
Struttura	Città	Stato o regione	Stato
University of Alberta Hospital	Edmonton	Alberta	In reclutamento
Hamilton Health Sciences - Hamilton General Hospital	Hamilton	Ontario	In reclutamento
Health Sciences North	Hamilton	Ontario	In reclutamento
Sunnybrook Research Institute	North York	Ontario	In reclutamento
Vancouver General Hospital	Vancouver	British Columbia	In reclutamento

France

France
Struttura	Città	Stato o regione	Stato
Hopital Pellegrin CHU Bordeaux	Bordeaux		In reclutamento
Aphm Hopital Timone	Marseille		In reclutamento
Chru Nancy Hopital Central	Nancy		In reclutamento
CHU Pontchaillou /Hopital Sud Service de Neurologie	Rennes	Brittany Region	In reclutamento
CHU Strasbourg Hopital de Hautepierre	Strasbourg		In reclutamento

Georgia

Georgia
Struttura	Città	Stato o regione	Stato
West Georgia Medical Center LTD	Kutaisi	Georgia	Attivo, non in reclutamento
Israel-Georgia Medical Research Clinic-Healthycore LTD	Tbilisi	Georgia	Attivo, non in reclutamento
New Hospitals LTD	Tbilisi	Georgia	Attivo, non in reclutamento
Pineo Medical Ecosystem LTD	Tbilisi	Georgia	Attivo, non in reclutamento
JSC K. Eristavi National Center of Experimental and Clinical Surgery	Tbilisi	Georgia	Attivo, non in reclutamento

Hungary

Hungary
Struttura	Città	Stato o regione	Stato
Bajcsy-Zsilinszky Hospital	Budapest	Hungary	In reclutamento
North Buda St. John Central Hospital	Budapest		Non ancora in reclutamento
Petz Aladár County Teaching Hospital	Győr	Vasvári Pál U. 2-4	In reclutamento
St. Damjan Greek Catholic Hospital	Kisvárda	Hungary	In reclutamento
B.-A.-Z. County Central Hospital	Miskolc	Hungary	In reclutamento

Poland

Poland
Struttura	Città	Stato
UCM, Katowice	Katowice	In reclutamento
University Hospital in Krakow	Krakow	In reclutamento
Szpital Czerniakowski Warsaw	Warsaw	In reclutamento
Military Institute of Medicine - National Research Institute	Warsaw	In reclutamento
4 Wojskowy Szpital Kliniczny z Polikliniką SP ZOZ we Wrocławiu	Wroclaw	In reclutamento
University Hospital of Zielona Góra	Zielona Góra	In reclutamento

Romania

Romania
Struttura	Città	Stato o regione	Stato
Fundeni Clinical Institute	Bucharest	Bucharest (Sector 2)	In reclutamento
Elias Emergency University Hospital	Bucharest	Romania	In reclutamento

Spain

Spain
Struttura	Città	Stato o regione	Stato
Instituto de Investigacion Biomedica de A Coruna (INIBIC)	A Coruña	Spain	In reclutamento
Hospital Universitario Germans Trias i Pujol	Badalona	Spain	In reclutamento
Hospital Universitari Vall d'Hebron-Institut de Recerca	Barcelona	Spain	In reclutamento
Hospital Clínico Universitario de Santiago	Santiago de Compostela	Spain	In reclutamento

United Kingdom

United Kingdom
Struttura	Città	Stato o regione	Stato
Addenbrooke's Hospital	Cambridge	United Kingdom	In reclutamento
Royal Devon and Exeter Hospital	Exeter	Devon	In reclutamento
Victoria Hospital- NHS Fife- Scotland- UK	Kirkcaldy		In reclutamento
Leeds Teaching Hospitals NHS Trust	Leeds		Non ancora in reclutamento
St George's Hospital	London	United Kingdom	In reclutamento
Barts Health NHS Trust The Royal London Hospital	London		In reclutamento
Charing Cross Hospital	London		In reclutamento
University College of London	London		In reclutamento
James Cook University Hospital	Middlesbrough		Non ancora in reclutamento
The Newcastle upon Tyne Hospitals NHS Foundation Trust - Royal Victoria Infirmary (RVI)	Newcastle upon Tyne	England	In reclutamento
Nottingham University Hospital	Nottingham		In reclutamento
Royal Stoke University Hospital	Stoke-on-Trent	United Kingdom	In reclutamento

Nella scheda del registro sono indicati altri 36 centri.

Documenti dello studio

In questa scheda del registro non sono collegati documenti.

Modifiche nel tempo

21 agosto 2026
Centro aggiunto
20 sites added (86 total)
6686

Registro: ClinicalTrials.gov · NCT########

https://xmedica.io/trials/ctgov/NCT05065216