Open-Label Expanded Access for Ebola-Infected Patients to Receive Human mAb Ansuvimab as Therapeutic or for HR PEP
Primary Purpose
Hemorrhagic Fever, Ebola
Status
Available
Phase
Locations
International
Study Type
Expanded Access
Intervention
Ansuvimab
Sponsored by
About this trial
This is an expanded access trial for Hemorrhagic Fever, Ebola focused on measuring Zaire ebolavirus, EVD, EBANGA, compassionate use
Eligibility Criteria
Inclusion Criteria:
- Male or female with laboratory confirmed (based on local standard of care) EBOV infection or with recent high-risk EBOV exposure as determined by a treating Physician or designee.
- Able to provide proof of identity to the satisfaction of the clinical team
- Able and willing to complete the informed consent process personally, or if the patient is unable to do so, then informed consent completed by a legally-authorized representative according to local laws and regulations.
Exclusion Criteria:
- Any medical condition that, in the opinion of the Treating Physician, would place the patient at an unreasonably increased risk through participation in this treatment protocol.
Sites / Locations
- Institut National de Recherche Biomedical
- Institut National de Recherche Biomedical
- Institut National de Recherche Biomédicale
- University of Sierra Leone Teaching Hospital Complex
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT05067166
First Posted
September 23, 2021
Last Updated
May 3, 2022
Sponsor
Ridgeback Biotherapeutics, LP
Collaborators
Institut National de Recherche Biomédicale. Kinshasa, République Démocratique du Congo
1. Study Identification
Unique Protocol Identification Number
NCT05067166
Brief Title
Open-Label Expanded Access for Ebola-Infected Patients to Receive Human mAb Ansuvimab as Therapeutic or for HR PEP
Official Title
Open-Label, Expanded Access Protocol of a Human Monoclonal Antibody, Ansuvimab (mAb114), Administered as an Investigational Therapeutic to Ebola-Infected Patients or as a High-Risk Ebola Post-Expo
Study Type
Expanded Access
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Available
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ridgeback Biotherapeutics, LP
Collaborators
Institut National de Recherche Biomédicale. Kinshasa, République Démocratique du Congo
4. Oversight
5. Study Description
Brief Summary
The human monoclonal antibody (mAb), ansuvimab (mAb114), will be provided to Ebola-infected patients as either a treatment or as PEP under expanded access. Ansuvimab is administered at 50 mg/kg as a single intravenous (IV) infusion
Detailed Description
This is an open-label, intermediate size patient population, expanded access protocol (EAP) of the ansuvimab investigational product administered once by IV infusion at a dose of about 50 mg/kg (weight-based dosing). Assessment of safety will include clinical observation and monitoring following administration. Patients will be monitored and assessed daily through discharge for safety and the incidence of serious adverse events (SAEs) and AEs that by clinical judgement are atypical for EVD, and any AEs that occur during product infusions. Blood will be collected for ansuvimab PK assessment, sGP quantification and RT-PCR evaluation of viral load by available assay. A blood sample for Ebolavirus viral load measurement is collected before mAb114 administration and at subsequent study timepoints per the Schedule of Evaluations. Subjects will be followed for up to 3 weeks after the product administration or until discharge from the Ebola Treatment Unit (ETU), whichever is later. Survival status for infected patients and/or EVD disease status for PEP subjects will be recorded as applicable. Ansuvimab will be provided for expanded access in the DRC and can be used in any DRC Ebolavirus (Zaire) outbreak location as authorized by the DRC Ministry of Health and the local Institutional Review Board.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhagic Fever, Ebola
Keywords
Zaire ebolavirus, EVD, EBANGA, compassionate use
7. Study Design
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Ansuvimab
Other Intervention Name(s)
mAb114, Ebanga
Intervention Description
single infusion 50 mg/kg IV
10. Eligibility
Sex
All
Eligibility Criteria
Inclusion Criteria:
Male or female with laboratory confirmed (based on local standard of care) EBOV infection or with recent high-risk EBOV exposure as determined by a treating Physician or designee.
Able to provide proof of identity to the satisfaction of the clinical team
Able and willing to complete the informed consent process personally, or if the patient is unable to do so, then informed consent completed by a legally-authorized representative according to local laws and regulations.
Exclusion Criteria:
- Any medical condition that, in the opinion of the Treating Physician, would place the patient at an unreasonably increased risk through participation in this treatment protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sabue Mulangu, MD,DTMH,PhD
Phone
1 833 846 3789
Email
EAP-requests@ridgebackbio.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Jacques Muyembe-Tamfum, MD,PhD
Organizational Affiliation
INRB
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut National de Recherche Biomedical
City
Mbandaka
State/Province
Equateur
Country
Congo, The Democratic Republic of the
Individual Site Status
Available
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Celestin Tshimanga, MD
Phone
18338463789
Email
EAP-requests@ridgebackbio.com
First Name & Middle Initial & Last Name & Degree
Bobo Bazola Nsemi, MD
Phone
18338463789
Email
EAP-requests@ridgebackbio.com
Facility Name
Institut National de Recherche Biomedical
City
Beni
State/Province
North Kivu
Country
Congo, The Democratic Republic of the
Individual Site Status
Available
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Celestin Tshimanga, MD
Phone
18338463789
Email
EAP-requests@ridgebackbio.com
First Name & Middle Initial & Last Name & Degree
Victor Malengera, MD
Phone
18338463789
Email
EAP-requests@ridgebackbio.com
Facility Name
Institut National de Recherche Biomédicale
City
Butembo
State/Province
North Kivu
Country
Congo, The Democratic Republic of the
Individual Site Status
Available
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Celestin Tshimanga, MD
Phone
18338463789
Email
EAP-requests@ridgebackbio.com
First Name & Middle Initial & Last Name & Degree
Jepsy Yango wa Yango, MD
Phone
18338463789
Email
EAP-requests@ridgebackbio.com
First Name & Middle Initial & Last Name & Degree
Victor Malengera, MD
Facility Name
University of Sierra Leone Teaching Hospital Complex
City
Freetown
Country
Sierra Leone
Individual Site Status
Available
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sulaiman Lakoh, MD
Phone
18338463789
Email
EAP-requests@ridgebackbio.com
12. IPD Sharing Statement
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Links:
URL
http://www.ridgebackbio.com
Description
Ridgeback Biotherapeutics (corporate website)
URL
https://www.inrb.net
Description
Institut National pour la Recherche Biomedicale
URL
https://apps.who.int/iris/handle/10665/250580
Description
WHO: Guidance for managing ethical issues in infectious disease outbreaks
Learn more about this trial
Open-Label Expanded Access for Ebola-Infected Patients to Receive Human mAb Ansuvimab as Therapeutic or for HR PEP
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