Back to resultsStudy to Evaluate the Efficacy and Safety of REGN3918 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
Primary Purpose
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
REGN3918
Sponsored by
About this trial
This is an interventional treatment trial for Paroxysmal Nocturnal Hemoglobinuria (PNH)
Eligibility Criteria
Key Inclusion Criteria:
- Diagnosis of paroxysmal nocturnal hemoglobinuria (PNH) confirmed by high-sensitivity flow cytometry
- PNH granulocytes > 10% at screening visit
- Active disease, as defined by the presence of 1 or more PNH-related signs or symptoms (eg, fatigue, hemoglobinuria, abdominal pain, shortness of breath [dyspnea], anemia [hemoglobin <10 g/dL], history of a MAVE [including thrombosis], dysphagia, or erectile dysfunction) or history of red blood cell (RBC) transfusion due to PNH within 3 months of screening.
- Lactate dehydrogenase (LDH) level ≥ 2 × upper limit of normal (ULN) at screening visit.
Key Exclusion Criteria:
- Prior treatment with a complement inhibitor either within 6 months prior to screening visit or at any time where the patient was refractory to complement inhibitor therapy, in the opinion of the investigator (with the exception of eculizumab refractory patients due to the C5 variant R885H/C)
- History of bone marrow transplantation
- Body weight < 40 kilograms at screening visit
- Peripheral blood absolute neutrophil count (ANC) <500/μL [<0.5 x 109/L] or peripheral blood platelet count <50,000/μL
- Documented history of systemic fungal disease or unresolved tuberculosis, or evidence of active or latent tuberculosis infection (LTBI) during screening period
- Any contraindication for receiving Neisseria meningitidis vaccination and antibiotic prophylaxis therapy as recommended in the study
- Any active, ongoing infection within 2 weeks of screening or during the screening period
- Any clinically significant abnormality identified at the time of screening that in the judgment of the Investigator or any sub-Investigator would preclude safe completion of the study or constrain endpoints assessment such as major systemic diseases, or patients with short life expectancy
- Women who are pregnant, breastfeeding, or who have a positive pregnancy test at screening visit or day 1
NOTE: Other protocol defined Inclusion/Exclusion criteria apply.
Sites / Locations
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
- Regeneron Study Site
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
REGN3918
Arm Description
Cohort A (Dose Confirmation) If a decision is made to expand Cohort A, patients will be assigned to Cohort A. Cohort B (Dose Expansion) If a decision is made to progress to Cohort B, patients will be assigned to Cohort B.
Outcomes
Primary Outcome Measures
Percentage of Participants Who Achieved Adequate Control of Intravascular Hemolysis
Participants were considered to have had adequate control of intravascular hemolysis if all of their lactose dehydrogenase (LDH) readings from Week 4 through Week 26 inclusive had values less than or equal to ≤ 1.5 × upper limit of normal (ULN). Participants must have greater than or equal to (≥) 50 percent (%) of scheduled LDH measures in those weeks, must not have had more than (>) 2 consecutive visits without LDH measures, must not have experienced breakthrough hemolysis, and must not have discontinued study treatment early. Participants were considered not to have had adequate control of intravascular hemolysis if they failed any of these criteria.
Percentage of Participants Who Achieved Transfusion Avoidance
Transfusion avoidance was defined as not having received red blood cell (RBC) transfusion during the first 26 weeks. A transfusion was counted only if it was per-protocol, that is, it followed the predefined transfusion algorithm: RBC transfusion due to a post-baseline hemoglobin level < 9 grams per deciliter (g/dL) (with anemia symptoms) or a post-baseline hemoglobin level < 7 g/dL (without anemia symptoms).
Secondary Outcome Measures
Percentage of Participants Who Had Breakthrough Hemolysis (BTH)
Breakthrough hemolysis was defined as the measurement of LDH ≥ 2 ULN concomitant with associated signs or symptoms at any time subsequent to an initial achievement of disease control (i.e., LDH ≤ 1.5 ULN).
Percentage of Participants Who Achieved Normalization of Intravascular Hemolysis
A participant was considered to have achieved normalization of intravascular hemolysis if their LDH readings between Week 4 through Week 26 inclusive had values ≤ 1.0 ULN. A participant must have ≥ 50% of scheduled LDH measures in those weeks, must not have had > 2 consecutive visits without LDH measures, must not have experienced breakthrough hemolysis, and must not have discontinued study treatment early. A participant was considered not to have achieved normalization of intravascular hemolysis if they failed any of these criteria.
Time to First Lactate Dehydrogenase (LDH) ≤1.5 x ULN
A time-to-first-event analysis was used to estimate the proportion of participants achieving transfusion avoidance at Week 26.
Percentage of Days With LDH ≤ 1.5 ULN From Week 4 Through Week 26
Percentage of days was calculated as number of days with LDH ≤ 1.5 x ULN divided by the participant's total treatment duration (total number of days on treatment from Week 4 through Week 26). LDH ≤ 1.5 x ULN was used as an indicator of adequate control of intravascular hemolysis.
Change From Baseline in LDH Levels at Week 26
Change from baseline in LDH levels at Week 26 was reported.
Percent Change From Baseline in LDH Levels at Week 26
Percent change from baseline in LDH levels at Week 26 was reported.
Rate of Transfusion With Red Blood Cells (RBCs)
The rate of transfusion with RBCs for a participant was the total number of transfusions divided by total person-years of time on treatment.
Number of Units of Transfusion With RBCs
Transfusions with RBCs proceeded according to the following predefined criteria that triggered a transfusion; however, the actual number of units to be transfused is at the discretion of the investigator: • Transfuse with RBC(s) if the post-baseline hemoglobin level is <9 g/dL with symptoms resulting from anemia or • Transfuse with RBC(s) if the post-baseline hemoglobin level is <7 g/dL.
Change From Baseline in RBC Hemoglobin Levels at Week 26
Hemoglobin levels in participants with PNH was measured. Change from baseline in RBC hemoglobin at Week 26 was reported.
Change From Baseline in Free Hemoglobin Levels at Week 26
Change from baseline in free hemoglobin levels at Week 26 was assessed.
Change From Baseline in Total Complement Hemolytic Activity Assay (CH50) at Week 26
Change from baseline in total CH50 at Week 26 was reported. Here "International units per milliliter" was abbreviated as "IU/mL".
Percent Change From Baseline in CH50 up to Week 26
Percent change from baseline in CH50 up to Week 26 was reported.
Change From Baseline in Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) at Week 26
The FACIT-F was a 13-item, self-reported PRO measure assessing an individual's level of fatigue during their usual daily activities over the past week. This questionnaire was part of the FACIT measurement system, a compilation of questions measuring health-related QoL in participants with cancer and other chronic illnesses. The FACIT-fatigue assessed the level of fatigue using a 4-point Likert scale ranging from 0 (not at all), 1 (a little bit), 2 (somewhat), 3 (quite a bit), 4 (very much) The sum of all responses resulted in the FACIT-F score for a total possible score of 0 to 52, with higher scores indicated greater fatigue.
Change From Baseline in the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-core 30 (EORTC QLQ-C30) at Week 26
The EORTC QLQ-C30 was a 30-item questionnaire used to assess symptoms and side effects of treatment and the impact on everyday life. It consists of 15 domains: 5 multi-item functioning scales (physical, role, social, emotional and cognitive), answered on a 4-point scale (1=Not at all,2=A Little,3=Quite a Bit,4=Very Much). Each score ranges from 0-100 with a higher score indicates higher level of functioning and a better QoL. A global health status/QoL scale that was answered on a 7-point scale (1=Very Poor to 7=Excellent). Each score ranges from 0-100 with a higher score indicates a better QoL. 9 symptom scales (Fatigue, Nausea and Vomiting, Pain, Dyspnea, Insomnia, Appetite Loss, Constipation, Diarrhea, Financial Impact), answered on a 4-point scale (1=Not at all, 2=A Little, 3=Quite a Bit, 4=Very Much). Each score ranges from 0 to 100 with a higher score indicates a higher level of symptoms, and a negative change from baseline indicates an improvement in symptoms.
Change From Baseline in European Quality of Life-5 Dimensions-3 Level (EQ-5D-3L) Index Score
EQ-5D-3L was a self-administered standardized instrument for use as measure of health outcome. It comprised 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension rated on 3 levels scale: 1 (no problems), 2 (some problems), 3 (extreme problems). The summed score ranges from 5-15 with "5" corresponding to no problems and "15" to severe problems in 5 dimensions. EQ-5D index calculated by applying preference-based weights (tariffs) to scores of five health state dimensions. Index values range from -1 to 1, with 0 representing a health state equivalent to death and 1 representing perfect health. Total index EQ-5D-3L summary score was weighted with a range of -0.594 (worst) to 1.0 (best).
Change From Baseline in EQ-5D-3L Visual Analogue Scale (VAS) at Week 26
The EQ-5D-3L was a standardized instrument for use as a measure of health outcome and was administered to all participants to assess the effect of the treatment on the participants' quality of life. The EQ-5D-3L includes a visual analog scale (VAS) which is a vertical scale with numbers ranging from 0 to 100. Participants were asked to draw a line to the place on the scale that best represented how good or bad his health was on that day. The worst state a participant can imagine was marked zero, and the best state the participant can imagine was marked 100. Mean change in VAS score from baseline was reported.
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious TEAEs
An adverse event (AE) was defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment. TEAEs was defined as AEs that developed or worsened during the on-treatment period. SAE was defined as any untoward medical occurrence that resulted in any of following outcomes: death, life-threatening, required initial/prolonged in-participant hospitalization, persistent/significant disability/incapacity, congenital anomaly/birth defect/considered as medically important event. TEAEs included both Serious TEAEs and non-serious TEAEs.
Number of Participants With TEAEs Based on Severity
An AE was defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment. Severity of AEs was graded according to the following scale, Mild: event that does not generally interfere with usual activities of daily living; Moderate: event that interferes with usual activities of daily living, causing discomfort, permanent risk of harm; Severe: AE that interrupts usual activities of daily living, significantly affects clinical status, or may require intensive therapeutic intervention.
Number of Participants With Clinically Meaningful Changes in Clinical Laboratory Parameters
Clinical laboratory parameters included biochemistry, hematology and urinalysis. Number of participants with potential clinically significant changes in laboratory parameters which were deemed clinically meaningful by the investigator were reported.
Number of Participants With Clinically Meaningful Changes in Vital Signs
Vital sign assessments included pulse rate, blood pressure (systolic and diastolic blood pressure) and body temperature. Number of participants with potential clinically meaningful changes in vital signs which were deemed clinically significant by the investigator were reported.
Number of Participants With Clinically Meaningful Changes in 12-lead Electrocardiograms (ECGs)
12-lead ECGs were evaluated. Any change in ECG assessments which are deemed clinically meaningful by the investigator were reported.
Serum Concentrations of Total REGN3918
Serum Concentrations of total REGN3918 was reported.
Number of Participants With Treatment-emergent Anti-Drug Antibodies (ADA) Response to REGN3918
Number of Participants with treatment-emergent ADA response to REGN3918 was reported.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03946748
Brief Title
Study to Evaluate the Efficacy and Safety of REGN3918 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
Official Title
An Open-Label, Single Arm Study to Evaluate the Efficacy and Safety of REGN3918 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Who Are Complement Inhibitor-Naive or Have Not Recently Received Complement Inhibitor Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
May 16, 2019 (Actual)
Primary Completion Date
June 9, 2021 (Actual)
Study Completion Date
June 10, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Regeneron Pharmaceuticals
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The primary objective of the study is to demonstrate a reduction in intravascular hemolysis by REGN3918 over 26 weeks of treatment in patients with active PNH who are treatment-naive to complement inhibitor therapy or have not recently received complement inhibitor therapy.
The secondary objectives of the study are:
To evaluate the safety and tolerability of REGN3918.
To evaluate the effect of REGN3918 on parameters of intravascular hemolysis
To assess the concentrations of total REGN3918 in serum.
To evaluate the incidence of treatment-emergent anti-drug antibodies to REGN3918 over time
To evaluate the effect of REGN3918 on patient-reported outcomes (PROs) measuring fatigue and health-related quality of life
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Paroxysmal Nocturnal Hemoglobinuria (PNH)
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
REGN3918
Arm Type
Experimental
Arm Description
Cohort A (Dose Confirmation) If a decision is made to expand Cohort A, patients will be assigned to Cohort A.
Cohort B (Dose Expansion) If a decision is made to progress to Cohort B, patients will be assigned to Cohort B.
Intervention Type
Drug
Intervention Name(s)
REGN3918
Intervention Description
Single intravenous (IV) dose, then a subcutaneous (SC) dose once weekly (QW).
Primary Outcome Measure Information:
Title
Percentage of Participants Who Achieved Adequate Control of Intravascular Hemolysis
Description
Participants were considered to have had adequate control of intravascular hemolysis if all of their lactose dehydrogenase (LDH) readings from Week 4 through Week 26 inclusive had values less than or equal to ≤ 1.5 × upper limit of normal (ULN). Participants must have greater than or equal to (≥) 50 percent (%) of scheduled LDH measures in those weeks, must not have had more than (>) 2 consecutive visits without LDH measures, must not have experienced breakthrough hemolysis, and must not have discontinued study treatment early. Participants were considered not to have had adequate control of intravascular hemolysis if they failed any of these criteria.
Time Frame
Week 4 through Week 26
Title
Percentage of Participants Who Achieved Transfusion Avoidance
Description
Transfusion avoidance was defined as not having received red blood cell (RBC) transfusion during the first 26 weeks. A transfusion was counted only if it was per-protocol, that is, it followed the predefined transfusion algorithm: RBC transfusion due to a post-baseline hemoglobin level < 9 grams per deciliter (g/dL) (with anemia symptoms) or a post-baseline hemoglobin level < 7 g/dL (without anemia symptoms).
Time Frame
Up to 26 Weeks
Secondary Outcome Measure Information:
Title
Percentage of Participants Who Had Breakthrough Hemolysis (BTH)
Description
Breakthrough hemolysis was defined as the measurement of LDH ≥ 2 ULN concomitant with associated signs or symptoms at any time subsequent to an initial achievement of disease control (i.e., LDH ≤ 1.5 ULN).
Time Frame
Baseline up to 26 Weeks
Title
Percentage of Participants Who Achieved Normalization of Intravascular Hemolysis
Description
A participant was considered to have achieved normalization of intravascular hemolysis if their LDH readings between Week 4 through Week 26 inclusive had values ≤ 1.0 ULN. A participant must have ≥ 50% of scheduled LDH measures in those weeks, must not have had > 2 consecutive visits without LDH measures, must not have experienced breakthrough hemolysis, and must not have discontinued study treatment early. A participant was considered not to have achieved normalization of intravascular hemolysis if they failed any of these criteria.
Time Frame
Week 4 through Week 26
Title
Time to First Lactate Dehydrogenase (LDH) ≤1.5 x ULN
Description
A time-to-first-event analysis was used to estimate the proportion of participants achieving transfusion avoidance at Week 26.
Time Frame
Up to Week 26
Title
Percentage of Days With LDH ≤ 1.5 ULN From Week 4 Through Week 26
Description
Percentage of days was calculated as number of days with LDH ≤ 1.5 x ULN divided by the participant's total treatment duration (total number of days on treatment from Week 4 through Week 26). LDH ≤ 1.5 x ULN was used as an indicator of adequate control of intravascular hemolysis.
Time Frame
Week 4 through Week 26
Title
Change From Baseline in LDH Levels at Week 26
Description
Change from baseline in LDH levels at Week 26 was reported.
Time Frame
Baseline, Week 26
Title
Percent Change From Baseline in LDH Levels at Week 26
Description
Percent change from baseline in LDH levels at Week 26 was reported.
Time Frame
Baseline, Week 26
Title
Rate of Transfusion With Red Blood Cells (RBCs)
Description
The rate of transfusion with RBCs for a participant was the total number of transfusions divided by total person-years of time on treatment.
Time Frame
Baseline up to Week 26
Title
Number of Units of Transfusion With RBCs
Description
Transfusions with RBCs proceeded according to the following predefined criteria that triggered a transfusion; however, the actual number of units to be transfused is at the discretion of the investigator: • Transfuse with RBC(s) if the post-baseline hemoglobin level is <9 g/dL with symptoms resulting from anemia or • Transfuse with RBC(s) if the post-baseline hemoglobin level is <7 g/dL.
Time Frame
Baseline up to Week 26
Title
Change From Baseline in RBC Hemoglobin Levels at Week 26
Description
Hemoglobin levels in participants with PNH was measured. Change from baseline in RBC hemoglobin at Week 26 was reported.
Time Frame
Baseline, Week 26
Title
Change From Baseline in Free Hemoglobin Levels at Week 26
Description
Change from baseline in free hemoglobin levels at Week 26 was assessed.
Time Frame
Baseline, Week 26
Title
Change From Baseline in Total Complement Hemolytic Activity Assay (CH50) at Week 26
Description
Change from baseline in total CH50 at Week 26 was reported. Here "International units per milliliter" was abbreviated as "IU/mL".
Time Frame
Baseline, Week 26
Title
Percent Change From Baseline in CH50 up to Week 26
Description
Percent change from baseline in CH50 up to Week 26 was reported.
Time Frame
Baseline up to Week 26
Title
Change From Baseline in Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) at Week 26
Description
The FACIT-F was a 13-item, self-reported PRO measure assessing an individual's level of fatigue during their usual daily activities over the past week. This questionnaire was part of the FACIT measurement system, a compilation of questions measuring health-related QoL in participants with cancer and other chronic illnesses. The FACIT-fatigue assessed the level of fatigue using a 4-point Likert scale ranging from 0 (not at all), 1 (a little bit), 2 (somewhat), 3 (quite a bit), 4 (very much) The sum of all responses resulted in the FACIT-F score for a total possible score of 0 to 52, with higher scores indicated greater fatigue.
Time Frame
Baseline, Week 26
Title
Change From Baseline in the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-core 30 (EORTC QLQ-C30) at Week 26
Description
The EORTC QLQ-C30 was a 30-item questionnaire used to assess symptoms and side effects of treatment and the impact on everyday life. It consists of 15 domains: 5 multi-item functioning scales (physical, role, social, emotional and cognitive), answered on a 4-point scale (1=Not at all,2=A Little,3=Quite a Bit,4=Very Much). Each score ranges from 0-100 with a higher score indicates higher level of functioning and a better QoL. A global health status/QoL scale that was answered on a 7-point scale (1=Very Poor to 7=Excellent). Each score ranges from 0-100 with a higher score indicates a better QoL. 9 symptom scales (Fatigue, Nausea and Vomiting, Pain, Dyspnea, Insomnia, Appetite Loss, Constipation, Diarrhea, Financial Impact), answered on a 4-point scale (1=Not at all, 2=A Little, 3=Quite a Bit, 4=Very Much). Each score ranges from 0 to 100 with a higher score indicates a higher level of symptoms, and a negative change from baseline indicates an improvement in symptoms.
Time Frame
Baseline, Week 26
Title
Change From Baseline in European Quality of Life-5 Dimensions-3 Level (EQ-5D-3L) Index Score
Description
EQ-5D-3L was a self-administered standardized instrument for use as measure of health outcome. It comprised 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension rated on 3 levels scale: 1 (no problems), 2 (some problems), 3 (extreme problems). The summed score ranges from 5-15 with "5" corresponding to no problems and "15" to severe problems in 5 dimensions. EQ-5D index calculated by applying preference-based weights (tariffs) to scores of five health state dimensions. Index values range from -1 to 1, with 0 representing a health state equivalent to death and 1 representing perfect health. Total index EQ-5D-3L summary score was weighted with a range of -0.594 (worst) to 1.0 (best).
Time Frame
Baseline, Week 26
Title
Change From Baseline in EQ-5D-3L Visual Analogue Scale (VAS) at Week 26
Description
The EQ-5D-3L was a standardized instrument for use as a measure of health outcome and was administered to all participants to assess the effect of the treatment on the participants' quality of life. The EQ-5D-3L includes a visual analog scale (VAS) which is a vertical scale with numbers ranging from 0 to 100. Participants were asked to draw a line to the place on the scale that best represented how good or bad his health was on that day. The worst state a participant can imagine was marked zero, and the best state the participant can imagine was marked 100. Mean change in VAS score from baseline was reported.
Time Frame
Baseline, Week 26
Title
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious TEAEs
Description
An adverse event (AE) was defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment. TEAEs was defined as AEs that developed or worsened during the on-treatment period. SAE was defined as any untoward medical occurrence that resulted in any of following outcomes: death, life-threatening, required initial/prolonged in-participant hospitalization, persistent/significant disability/incapacity, congenital anomaly/birth defect/considered as medically important event. TEAEs included both Serious TEAEs and non-serious TEAEs.
Time Frame
Baseline up to Week 26
Title
Number of Participants With TEAEs Based on Severity
Description
An AE was defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment. Severity of AEs was graded according to the following scale, Mild: event that does not generally interfere with usual activities of daily living; Moderate: event that interferes with usual activities of daily living, causing discomfort, permanent risk of harm; Severe: AE that interrupts usual activities of daily living, significantly affects clinical status, or may require intensive therapeutic intervention.
Time Frame
Baseline up to Week 26
Title
Number of Participants With Clinically Meaningful Changes in Clinical Laboratory Parameters
Description
Clinical laboratory parameters included biochemistry, hematology and urinalysis. Number of participants with potential clinically significant changes in laboratory parameters which were deemed clinically meaningful by the investigator were reported.
Time Frame
Baseline up to Week 26
Title
Number of Participants With Clinically Meaningful Changes in Vital Signs
Description
Vital sign assessments included pulse rate, blood pressure (systolic and diastolic blood pressure) and body temperature. Number of participants with potential clinically meaningful changes in vital signs which were deemed clinically significant by the investigator were reported.
Time Frame
Baseline up to Week 26
Title
Number of Participants With Clinically Meaningful Changes in 12-lead Electrocardiograms (ECGs)
Description
12-lead ECGs were evaluated. Any change in ECG assessments which are deemed clinically meaningful by the investigator were reported.
Time Frame
Baseline up to Week 26
Title
Serum Concentrations of Total REGN3918
Description
Serum Concentrations of total REGN3918 was reported.
Time Frame
Pre-dose (Day 0), End of infusion at Days 0, 2, 7, 28, 56, 84, 112, 140, and 182
Title
Number of Participants With Treatment-emergent Anti-Drug Antibodies (ADA) Response to REGN3918
Description
Number of Participants with treatment-emergent ADA response to REGN3918 was reported.
Time Frame
Baseline up to Week 26
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria:
Diagnosis of paroxysmal nocturnal hemoglobinuria (PNH) confirmed by high-sensitivity flow cytometry
PNH granulocytes > 10% at screening visit
Active disease, as defined by the presence of 1 or more PNH-related signs or symptoms (eg, fatigue, hemoglobinuria, abdominal pain, shortness of breath [dyspnea], anemia [hemoglobin <10 g/dL], history of a MAVE [including thrombosis], dysphagia, or erectile dysfunction) or history of red blood cell (RBC) transfusion due to PNH within 3 months of screening.
Lactate dehydrogenase (LDH) level ≥ 2 × upper limit of normal (ULN) at screening visit.
Key Exclusion Criteria:
Prior treatment with a complement inhibitor either within 6 months prior to screening visit or at any time where the patient was refractory to complement inhibitor therapy, in the opinion of the investigator (with the exception of eculizumab refractory patients due to the C5 variant R885H/C)
History of bone marrow transplantation
Body weight < 40 kilograms at screening visit
Peripheral blood absolute neutrophil count (ANC) <500/μL [<0.5 x 109/L] or peripheral blood platelet count <50,000/μL
Documented history of systemic fungal disease or unresolved tuberculosis, or evidence of active or latent tuberculosis infection (LTBI) during screening period
Any contraindication for receiving Neisseria meningitidis vaccination and antibiotic prophylaxis therapy as recommended in the study
Any active, ongoing infection within 2 weeks of screening or during the screening period
Any clinically significant abnormality identified at the time of screening that in the judgment of the Investigator or any sub-Investigator would preclude safe completion of the study or constrain endpoints assessment such as major systemic diseases, or patients with short life expectancy
Women who are pregnant, breastfeeding, or who have a positive pregnancy test at screening visit or day 1
NOTE: Other protocol defined Inclusion/Exclusion criteria apply.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clinical Trial Management
Organizational Affiliation
Regeneron Pharmaceuticals
Official's Role
Study Director
Facility Information:
Facility Name
Regeneron Study Site
City
Sha Tin
Country
Hong Kong
Facility Name
Regeneron Study Site
City
Budapest
ZIP/Postal Code
1083
Country
Hungary
Facility Name
Regeneron Study Site
City
Kaposvár
ZIP/Postal Code
4400
Country
Hungary
Facility Name
Regeneron Study Site
City
Seoul
ZIP/Postal Code
03080
Country
Korea, Republic of
Facility Name
Regeneron Study Site
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
Facility Name
Regeneron Study Site
City
Seoul
ZIP/Postal Code
05030
Country
Korea, Republic of
Facility Name
Regeneron Study Site
City
Seoul
ZIP/Postal Code
06351
Country
Korea, Republic of
Facility Name
Regeneron Study Site
City
Seoul
ZIP/Postal Code
07985
Country
Korea, Republic of
Facility Name
Regeneron Study Site
City
Kota Bharu
State/Province
Kelantan
ZIP/Postal Code
15586
Country
Malaysia
Facility Name
Regeneron Study Site
City
Sibu
State/Province
Sarawak
ZIP/Postal Code
96000
Country
Malaysia
Facility Name
Regeneron Study Site
City
Kuala Terengganu
State/Province
Terengganu
ZIP/Postal Code
20400
Country
Malaysia
Facility Name
Regeneron Study Site
City
Airdrie
State/Province
Lanarkshire
ZIP/Postal Code
ML60JS
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
All Individual Patient Data (IPD) that underlie publicly available results will be considered for sharing
IPD Sharing Time Frame
Individual anonymized participant data will be considered for sharing once the indication has been approved by a regulatory body, if there is legal authority to share the data and there is not a reasonable likelihood of participant re-identification.
IPD Sharing Access Criteria
Qualified researchers may request access to anonymized patient level data or aggregate study data when Regeneron has received marketing authorization from major health authorities (e.g., FDA, European Medicines Agency [EMA], Pharmaceuticals and Medical Devices Agency [PMDA], etc) for the product and indication, has the legal authority to share the data, and has made the study results publicly available (eg, scientific publication, scientific conference, clinical trial registry).
IPD Sharing URL
https://vivli.org/
Learn more about this trial
Study to Evaluate the Efficacy and Safety of REGN3918 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
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