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A Study to Determine the Efficacy and Safety of DNL310 vs Idursulfase in Pediatric Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II) (COMPASS)

Primary Purpose

Mucopolysaccharidosis II

Status
Recruiting
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
DNL310
Idursulfase
Sponsored by
Denali Therapeutics Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mucopolysaccharidosis II focused on measuring Hunter Syndrome, MPS II, nMPS II, nnMPS II

Eligibility Criteria

2 Years - 16 Years (Child)All SexesDoes not accept healthy volunteers

Key Inclusion Criteria:

  • Participants aged ≥2 to <6 years (Cohort A) or ≥6 to <17 years (Cohort B)
  • Confirmed diagnosis of MPS II (for Cohort A, nMPS II; for Cohort B, nnMPS II)
  • Be on maintenance enzyme replacement therapy (ERT) and have tolerated idursulfase for a minimum of 4 months prior to screening

Key Exclusion Criteria:

  • Have a documented mutation of other genes or genetic diagnosis accounting for developmental delay
  • Previously received an iduronate 2-sulfatase (IDS) gene therapy or stem cell therapy
  • Received any CNS-targeted MPS ERT within 6 months prior to screening
  • Have a contraindication for lumbar punctures and/or magnetic resonance imagings (MRIs)
  • Participated in any other investigational drug study or used an investigational drug within 60 days prior to screening or intend to receive another investigational drug during the study

Sites / Locations

  • UCSF Benioff Children's Hospital OaklandRecruiting
  • Emory UniversityRecruiting
  • Ann and Robert H Lurie Children's Hospital of ChicagoRecruiting
  • Hackensack University Medical CenterRecruiting
  • UNC Children's Research InstituteRecruiting
  • Cincinnati Children's Hospital Medical CenterRecruiting
  • Children's Hospital of PhiladelphiaRecruiting
  • Children's Hospital of PittsburghRecruiting
  • The University of Texas Medical School at HoustonRecruiting
  • Hospital Italiano de Buenos AiresRecruiting
  • Universitair Ziekenhuis BrusselRecruiting
  • UZ AntwerpenRecruiting
  • University of Alberta - Faculty of Medicine & DentistryRecruiting
  • Hospital for Sick ChildrenRecruiting
  • McGill University Health CenterRecruiting
  • Vseobecna Fakultni Nemocnice V PrazeRecruiting
  • Hôpital Jeanne de FlandreRecruiting
  • Hopitaux de La TimoneRecruiting
  • CHU ToulouseRecruiting
  • Universitätsklinikum Hamburg EppendorfRecruiting
  • SphinCSRecruiting
  • Azienda Ospedaliera Universitaria Federico IIRecruiting
  • Azienda Sanitaria Universitaria Friuli Centrale - PO Universitario Santa Maria della MisericordiaRecruiting
  • Erasmus Medical Center - Sophia Children's HospitalRecruiting
  • Hospital Clínico Universitario de SantiagoRecruiting
  • Hospital Universitario Vall d'HebronRecruiting
  • Hospital Infantil Universitario Niño JesusRecruiting
  • Drottning Silvias Barn Och UngdomssjukhusRecruiting
  • Cukurova University Medical Faculty Balcali HospitalRecruiting
  • Gazi Universitesi Tip FakultesiRecruiting
  • Birmingham Women's and Children's NHS Foundation TrustRecruiting
  • Great Ormond Street Hospital for ChildrenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Cohort A: Participants with nMPS II

Cohort B: Participants with nnMPS II

Open-label Treatment Phase

Arm Description

Participants who meet pre-specified criteria may receive DNL310 or idursulfase

Outcomes

Primary Outcome Measures

Percent change from baseline in cerebrospinal fluid (CSF) heparan sulfate (HS) concentration (Cohort A only)
Change from baseline in the Vineland Adaptive Behavior Scale, Third Edition (Vineland-3)(Cohort A only)

Secondary Outcome Measures

Change from baseline in the Bayley Scales of Infant and Toddler Development, Third Edition (BSID-III)(Cohort A only)
Change from baseline in distance walked in the Six-Minute Walk Test (6MWT; Cohort B only)
Percent change from baseline in the sum of urine HS and dermatan sulfate (DS) concentrations (Cohorts A and B)
Liver volume within the normal range (normal vs abnormal) as measured by magnetic resonance imaging (MRI) (Cohorts A and B)
Spleen volume within the normal range (normal vs abnormal) as measured by MRI (Cohorts A and B)
Improvement in Parent/Caregiver Global Impression of Change (CaGI-C) Overall MPS II (Cohorts A and B)

Full Information

First Posted
May 9, 2022
Last Updated
September 27, 2023
Sponsor
Denali Therapeutics Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05371613
Brief Title
A Study to Determine the Efficacy and Safety of DNL310 vs Idursulfase in Pediatric Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II)
Acronym
COMPASS
Official Title
A Phase 2/3, Multicenter, Double-Blind, Randomized Study to Determine the Efficacy and Safety of DNL310 vs Idursulfase in Pediatric Participants With Neuronopathic or Non-Neuronopathic Mucopolysaccharidosis Type II
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 21, 2022 (Actual)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Denali Therapeutics Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a Phase 2/3, multiregional, two-arm, double-blind, randomized, active (standard-of-care)-controlled study of the efficacy and safety of DNL310, an investigational central nervous system (CNS)-penetrant enzyme-replacement therapy (ERT) for mucopolysaccharidosis type II (MPS II). Participants may also qualify to enter an open-label treatment phase with DNL310 or idursulfase based on pre-specified criteria.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mucopolysaccharidosis II
Keywords
Hunter Syndrome, MPS II, nMPS II, nnMPS II

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
54 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cohort A: Participants with nMPS II
Arm Type
Experimental
Arm Title
Cohort B: Participants with nnMPS II
Arm Type
Experimental
Arm Title
Open-label Treatment Phase
Arm Type
Experimental
Arm Description
Participants who meet pre-specified criteria may receive DNL310 or idursulfase
Intervention Type
Drug
Intervention Name(s)
DNL310
Intervention Description
Intravenous repeating dose
Intervention Type
Drug
Intervention Name(s)
Idursulfase
Intervention Description
Intravenous repeating dose
Primary Outcome Measure Information:
Title
Percent change from baseline in cerebrospinal fluid (CSF) heparan sulfate (HS) concentration (Cohort A only)
Time Frame
24 weeks
Title
Change from baseline in the Vineland Adaptive Behavior Scale, Third Edition (Vineland-3)(Cohort A only)
Time Frame
96 weeks
Secondary Outcome Measure Information:
Title
Change from baseline in the Bayley Scales of Infant and Toddler Development, Third Edition (BSID-III)(Cohort A only)
Time Frame
96 weeks
Title
Change from baseline in distance walked in the Six-Minute Walk Test (6MWT; Cohort B only)
Time Frame
48 weeks
Title
Percent change from baseline in the sum of urine HS and dermatan sulfate (DS) concentrations (Cohorts A and B)
Time Frame
up to 48 weeks
Title
Liver volume within the normal range (normal vs abnormal) as measured by magnetic resonance imaging (MRI) (Cohorts A and B)
Time Frame
48 weeks
Title
Spleen volume within the normal range (normal vs abnormal) as measured by MRI (Cohorts A and B)
Time Frame
48 weeks
Title
Improvement in Parent/Caregiver Global Impression of Change (CaGI-C) Overall MPS II (Cohorts A and B)
Time Frame
48 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria: Participants aged ≥2 to <6 years (Cohort A) or ≥6 to <17 years (Cohort B) Confirmed diagnosis of MPS II (for Cohort A, nMPS II; for Cohort B, nnMPS II) Be on maintenance enzyme replacement therapy (ERT) and have tolerated idursulfase for a minimum of 4 months prior to screening Key Exclusion Criteria: Have a documented mutation of other genes or genetic diagnosis accounting for developmental delay Previously received an iduronate 2-sulfatase (IDS) gene therapy or stem cell therapy Received any CNS-targeted MPS ERT within 6 months prior to screening Have a contraindication for lumbar punctures and/or magnetic resonance imagings (MRIs) Participated in any other investigational drug study or used an investigational drug within 60 days prior to screening or intend to receive another investigational drug during the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Clinical Trials at Denali Therapeutics
Email
clinical-trials@dnli.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lubica Trokan, MD, MPH
Organizational Affiliation
Denali Therapeutics Inc.
Official's Role
Study Director
Facility Information:
Facility Name
UCSF Benioff Children's Hospital Oakland
City
Oakland
State/Province
California
ZIP/Postal Code
94609
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annie Sako
Phone
510-428-3885
Ext
4785
Email
annie.sako@ucsf.edu
First Name & Middle Initial & Last Name & Degree
Paul Harmatz, MD
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gwendolyn Gunn
Email
gwendolyn.gisiner.gunn@emory.edu
First Name & Middle Initial & Last Name & Degree
William Wilcox, MD
Facility Name
Ann and Robert H Lurie Children's Hospital of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lindsey Lang
Email
llang@luriechildrens.org
Phone
312-227-6712
First Name & Middle Initial & Last Name & Degree
Barbara Burton, MD
Facility Name
Hackensack University Medical Center
City
Hackensack
State/Province
New Jersey
ZIP/Postal Code
07601
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susan Mathus
Email
susan.mathus@hmhn.org
First Name & Middle Initial & Last Name & Degree
Helio Pedro, MD
Facility Name
UNC Children's Research Institute
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27514
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Heather Press
Email
heather_preiss@med.unc.edu
First Name & Middle Initial & Last Name & Degree
Joseph Muenzer, MD
Facility Name
Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Connie Wehmeyer
Phone
513-636-4760
Email
connie.wehmeyer@cchmc.org
First Name & Middle Initial & Last Name & Degree
Nancy Leslie, MD
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Henry Daumeyer
Email
daumeyerh@chop.edu
First Name & Middle Initial & Last Name & Degree
Can Ficicioglu, MD
Facility Name
Children's Hospital of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15224
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dawn Kolar
Email
kolardr@upmc.edu
First Name & Middle Initial & Last Name & Degree
Deepa Rajan, MD
Facility Name
The University of Texas Medical School at Houston
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marilyn Garcia
Email
marilyn.garcia@uth.tmc.edu
First Name & Middle Initial & Last Name & Degree
Paul Hillman, MD
Facility Name
Hospital Italiano de Buenos Aires
City
Buenos Aires
ZIP/Postal Code
C1199ABB
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sabina Garcia
Email
sabinagarcia@iadin.com.ar
First Name & Middle Initial & Last Name & Degree
Javier Muntadas Rausei, MD
Facility Name
Universitair Ziekenhuis Brussel
City
Jette
State/Province
Brussels
ZIP/Postal Code
1090
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Raquel Van den Eydne
Email
Raquel.VanDenEynde@uzbrussel.be
First Name & Middle Initial & Last Name & Degree
Luc Regal, MD
Facility Name
UZ Antwerpen
City
Antwerpen
ZIP/Postal Code
2650
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tine Maes
Email
tine.maes@uza.be
First Name & Middle Initial & Last Name & Degree
Francois Eyskens, MD
Facility Name
University of Alberta - Faculty of Medicine & Dentistry
City
Edmonton
State/Province
Alberta
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Farah Hassan
Email
farah.hassan@albertahealthservices.ca
First Name & Middle Initial & Last Name & Degree
Saadet Andrews, MD
Facility Name
Hospital for Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G1X8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Preet Dhillon
Email
preet.dhillon@sickkids.ca
First Name & Middle Initial & Last Name & Degree
Michal Inbar-Feigenberg, MD
Facility Name
McGill University Health Center
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4A3J1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christine Gannon
Email
christine.gannon@muhc.mcgill.ca
First Name & Middle Initial & Last Name & Degree
John Mitchell, MD
Facility Name
Vseobecna Fakultni Nemocnice V Praze
City
Praha
ZIP/Postal Code
128 08
Country
Czechia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lenka Linkova
Email
lenka.linkova@vfn.cz
First Name & Middle Initial & Last Name & Degree
Martin Magner, MD
Facility Name
Hôpital Jeanne de Flandre
City
Lille
ZIP/Postal Code
59000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Celine Desopper
Email
amina.ziouche@chru-lillie.fr
First Name & Middle Initial & Last Name & Degree
Anne-Sophie Guémann, MD
Facility Name
Hopitaux de La Timone
City
Marseille
ZIP/Postal Code
13385
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Murielle Champeaux
Email
murielle.champeaux@ap-hm.fr
First Name & Middle Initial & Last Name & Degree
Brigitte Chabrol, MD
Facility Name
CHU Toulouse
City
Toulouse
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Léa Saintouil
Email
saintouil.l@chu-toulouse.fr
First Name & Middle Initial & Last Name & Degree
Aurélie Bourchany, MD
Facility Name
Universitätsklinikum Hamburg Eppendorf
City
Hamburg
ZIP/Postal Code
20251
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katharina Trepner
Email
icld@uke.de
First Name & Middle Initial & Last Name & Degree
Nicole Muschol, MD
Facility Name
SphinCS
City
Hochheim
ZIP/Postal Code
65239
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Loreen Gramsch
Email
loreen.gramsch@sphincs.de
First Name & Middle Initial & Last Name & Degree
Eugen Mengel, MD
Facility Name
Azienda Ospedaliera Universitaria Federico II
City
Napoli
ZIP/Postal Code
80131
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Margherita Dell'Anno
Email
m.dellanno@tigem.it
First Name & Middle Initial & Last Name & Degree
Giancarlo Parenti, MD
Facility Name
Azienda Sanitaria Universitaria Friuli Centrale - PO Universitario Santa Maria della Misericordia
City
Udine
ZIP/Postal Code
33100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Enrica Epifani
Email
enrica.epifani@asufc.sanita.fvg.it
First Name & Middle Initial & Last Name & Degree
Maurizio Scarpa, MD
Facility Name
Erasmus Medical Center - Sophia Children's Hospital
City
Rotterdam
ZIP/Postal Code
3000
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dorine Heemskerk
Email
t.heemskerk@erasmusmc.nl
First Name & Middle Initial & Last Name & Degree
Hannerieke van den Hout
Facility Name
Hospital Clínico Universitario de Santiago
City
A Coruña
ZIP/Postal Code
15706
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roi Chans Gerpe
Email
roi.chans.gerpe@sergas.es
First Name & Middle Initial & Last Name & Degree
Maria Luz Couce Pico, MD
Facility Name
Hospital Universitario Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marina González Riera
Email
marina.gonzalez@vhir.org
First Name & Middle Initial & Last Name & Degree
Mireia del Toro, MD
Facility Name
Hospital Infantil Universitario Niño Jesus
City
Madrid
ZIP/Postal Code
28009
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christiana Calvo Patino
Email
ccpatino@salud.madrid.org
First Name & Middle Initial & Last Name & Degree
Beatriz Bermadino, MD
Facility Name
Drottning Silvias Barn Och Ungdomssjukhus
City
Göteborg
ZIP/Postal Code
416 85
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tina Kjellén
Email
tina.kjellen@vgregion.se
First Name & Middle Initial & Last Name & Degree
Niklas Darin, MD, PhD
Facility Name
Cukurova University Medical Faculty Balcali Hospital
City
Adana
ZIP/Postal Code
1330
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nurşah Gulseren
Email
nursahgulseren523@hotmail.com
First Name & Middle Initial & Last Name & Degree
Neslihan Mungan, MD
Facility Name
Gazi Universitesi Tip Fakultesi
City
Çankaya
ZIP/Postal Code
06500
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gozde Dulgar
Email
gozde.dulgar@medex-smo.com
First Name & Middle Initial & Last Name & Degree
Faith Ezgu, MD
Facility Name
Birmingham Women's and Children's NHS Foundation Trust
City
Birmingham
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shashi Watson-Jones
Email
shashi.rana@nhs.net
First Name & Middle Initial & Last Name & Degree
Harprit Thakur
Email
harprit.thakur@nhs.net
Facility Name
Great Ormond Street Hospital for Children
City
London
ZIP/Postal Code
WC1N 3JH
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kerry Gilroy
Email
kerry.gilroy@gosh.nhs.uk
First Name & Middle Initial & Last Name & Degree
Olivia Rosie-Wilkinson
Email
Olivia.Rosie-Wilkinson@gosh.nhs.uk
First Name & Middle Initial & Last Name & Degree
Spyros Batzios, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://www.engagehunter.com/clinical-trials
Description
Engage Hunter Website

Learn more about this trial

A Study to Determine the Efficacy and Safety of DNL310 vs Idursulfase in Pediatric Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II)

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