Study to Evaluate the Efficacy and Safety of Suptavumab (REGN2222) for the Prevention of Medically Attended RSV (Respiratory Syncytial Virus) Infection in Preterm Infants

Phase 3

Completed

Conditions: Respiratory Syncytial Virus Infections

Interventions: Drug: Suptavumab 30 mg/kg- 1 Dose
Drug: Suptavumab 30 mg/kg
Drug: Placebo Matched to Suptavumab
Drug: Suptavumab 30 mg/kg - 2 Doses

Registration Number: NCT02325791

Lead Sponsor: Regeneron Pharmaceuticals

Brief Summary: The purpose of this study was to evaluate the efficacy, safety, pharmacokinetics (PK), and immunogenicity of suptavumab (REGN2222) in infants born no more than 35 weeks, 6 days gestational age who are no more than 6 months of age at the time of enrollment in their respective geographic location. In order to optimize the potential benefit in this vulnerable population, we conducted this study during the RSV season using dosing regimens that are expected to be effective.

Detailed Description: This study occurred in two parts: Part A and Part B.

Part A of the study was an open-label, PK evaluation of intramuscular (IM) administered suptavumab in preterm infants for whom palivizumab was not recommended to enable the selection of dosing regimens for Part B.

Part B of the study was randomized, double-blind, and placebo-controlled, designed to evaluate efficacy, safety, serum concentration and immunogenicity of IM administration of suptavumab in preterm infants for whom palivizumab was not recommended. The total duration of Part B was up to 265 days (includes a 28-day screening period, 57-day treatment period and 180-day follow-up period).

Up to 1515 subjects were planned to be included in Part B of the study. Participants were randomly assigned to 1 of 3 different groups, each with 505 infants; one group received one dose of suptavumab and one dose of placebo, the second group received two doses of suptavumab, and the third group received two doses of placebo.

There was a separate genetic testing sub study.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 1177

Inclusion Criteria

Preterm, otherwise healthy male or female infant who is ≤6 months of age at the time of the first dose (i.e., infant must be treated on or before their 6 month birthday)
Gestational age is ≤35 weeks, 6 days at birth
Parent(s) or legal guardian(s) of the infant is able to understand the study requirements and willing to provide informed consent

Key

Exclusion Criteria

Eligible, recommended and have access to receive palivizumab per AAP or other local guidelines, standard practice, or by their healthcare provider
History of CLD defined as requirement of supplemental oxygen for 28 days after birth
Known hemodynamically significant congenital heart disease
Known immunodeficiency, neuromuscular disease, or congenital abnormalities of the airway
Known renal or hepatic dysfunction
Major congenital malformations, including congenital cleft palate, cytogenetic abnormalities, or serious chronic disorders
Known or suspected impairment of immunological functions or autoimmune diseases
History of anaphylaxis
Previously received palivizumab or any other investigational RSV prophylaxis or vaccine product
Previous reaction to IV immunoglobulin, blood products or other foreign proteins, including vaccines and monoclonal antibodies

Note: Other inclusion and exclusion criteria apply

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Part B: Suptavumab 30 mg/kg- 1 Dose	Suptavumab 30 mg/kg- 1 Dose	-
Part A: Suptavumab 30 mg/kg	Suptavumab 30 mg/kg	-
Part B: Placebo Matched to Suptavumab	Placebo Matched to Suptavumab	-
Part B: Suptavumab 30 mg/kg - 2 Doses	Suptavumab 30 mg/kg - 2 Doses	-

Primary Outcome Measures

Name	Time	Method
Part A: Serum Concentration of Suptavumab Over Time	Day 1 through Day 150	Part A was primarily designed to determine the pharmacokinetics (PK) of suptavumab in infants to inform the dose regimen used in Part B of the study. The study protocol specified the process and criteria for assessment of the dose. The dose used in Part B was to remain the same as Part A if the PK data up to Day 57 demonstrated that the individual PK observations were consistent with model-predicted concentrations, following age and body weight corrections.
Part B: Percentage of Participants With Medically Attended Respiratory Syncytial Virus (RSV) Infection (Hospitalization or Outpatient Visit With Lower Respiratory Tract Infection [LRTI]) Up to Day 150	From first study drug administration up to Day 150	A medically attended RSV infection defined as an infant with positive RSV test by Reverse-transcriptase polymerase chain reaction (RT-PCR) with any of following events: Hospitalized (on basis of assessment of admitting physician) for RSV infection or outpatient visit (emergency room \[ER\], urgent care \[UC\], or pediatric clinic visits \[for either a sick or well visit\]) with RSV lower respiratory tract infection (LRTI). An RSV LRTI in an infant: RSV proven respiratory infection (i.e positive RSV RT-PCR test) with parent(s)/guardian(s) report of cough/difficulty breathing, \& with 1 of following signs of LRTI, as assessed by healthcare provider: - lower chest wall in drawing -hypoxemia (peripheral capillary oxygen saturation \<95% breathing room air) - Wheezing/crackles. The 150-day efficacy assessment period: first study drug intake through the Day 150 visit.

Secondary Outcome Measures

Name	Time	Method
Part A: Percentage of Participants With Treatment-Emergent Adverse Events (TEAEs)	Baseline through Day 150	Any untoward medical occurrence in participants, who received investigational medicinal product (IMP) was considered an adverse event (AE) without regard to possibility of causal relationship with this treatment. TEAEs: AEs that developed/worsened/became serious during on-treatment period (defined as time between the date of first study drug administration \& date of end of study/last visit).Serious AE: Any untoward medical occurrence that resulted in any of following outcomes: death, life-threatening, required initial or prolonged in-patient hospitalization, persistent/significant disability/incapacity, congenital anomaly/birth defect, or considered as medically important event. Any TEAE included participants with both serious \& non-serious AEs. National Cancer Institute Common Terminology Criteria (NCI-CTCAE) version 4.03(Grade 3 \[severe\] \& Grade 4\[life-threatening\]) was used in this study to grade clinical AEs.
Part B: Number of Participants With At Least One Positive Anti-Drug Antibody (ADA) Assay	Day 1 through Day 150	ADA category of each participant was classified as pre-existing immunoreactivity (a positive ADA response at baseline with a \<4-fold increase in titer for all post baseline samples), treatment-boosted (a positive response at baseline with at least one post baseline titer at \>=4-fold the baseline titer), or treatment-emergent (TE \[any positive post baseline assay response when baseline results were negative or missing\]). TE ADA responses were further classified as persistent (treatment-emergent positive ADA response detected in at least 2 consecutive post baseline samples separated by at least a 12-week post baseline period \[based on nominal sampling time\], with no ADA-negative samples in-between, regardless of any missing samples or a positive response at the last ADA sampling time point), indeterminate (a positive assay response at the last collection time point only, regardless of any missing samples), or transient (not persistent/indeterminate, regardless of any missing samples).
Part B: Serum Concentration of Suptavumab	Day 29, 57, 85, 113 and Day 150 Post-dose	Serum samples for drug concentration will be collected at pre-specified time points
Part B: Percentage of Participants Hospitalized With Medically Attended RSV Infection or Outpatient Visit Lower Respiratory Tract Infection (LRTI) or Upper Respiratory Tract Infection (URTI) Up to Day 150	From the first study drug administration up to Day 150	A medically attended RSV infection was defined as an infant with a positive RSV test by RT-PCR with any of the following events: -Hospitalized (on the basis of the assessment of the admitting physician) for RSV infection - or Outpatient visit (ER, UC), or pediatric clinic visits \[for either a sick or well visit\]) with RSV LRTI. An RSV LRTI in an infant: RSV-proven respiratory infection (i.e, positive RSV RT-PCR test) with parent(s)/guardian(s) report of cough or difficulty breathing, and with 1 of the following signs of LRTI, as assessed by a healthcare provider: -Lower chest wall indrawing -Hypoxemia (peripheral capillary oxygen saturation \<95% breathing room air) -Wheezing or crackles. The 150-day efficacy assessment period:first study drug intake through the Day 150 visit.