Evidence map›Paper›PMID 33411992›Full record

Trial reportClinical pharmacology in drug development2021

A Pharmacokinetic Bioequivalence Study of Fremanezumab Administered Subcutaneously Using an Autoinjector and a Prefilled Syringe.

Irina Cherniakov, Orit Cohen-Barak, Ryan Tiver, Michael Gillespie, Yoel Kessler, Maria Gutierrez, Michele Rasamoelisolo, Shawn Li, Honglue Shen, Hussein Hallak and 4 more

Open access · hybridAbstract readClinical Trial, Phase IComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology in drug development, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.0field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Clinical Qualification of Subcutaneous Injection Devices for Monoclonal Antibodies.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 4 countries.

Irina CherniakovSpecialty Clinical Development, Teva Pharmaceutical Industries Ltd, Netanya, Israel.
Orit Cohen-BarakSpecialty Clinical Development, Teva Pharmaceutical Industries Ltd, Netanya, Israel.
Ryan TiverSpecialty Clinical Development Teva Branded Pharmaceutical Products R&D, West Chester, Pennsylvania, USA.
Michael GillespieSpecialty Clinical Development Teva Branded Pharmaceutical Products R&D, West Chester, Pennsylvania, USA.
Yoel KesslerSpecialty Clinical Development, Teva Pharmaceutical Industries Ltd, Netanya, Israel.
Maria GutierrezTeva Internal Clinics US, Miramar, Florida, USA.
Michele RasamoelisoloNonclinical Development Teva Pharmaceutical Industries Ltd, West Chester, Pennsylvania, USA.
Shawn LiNonclinical Development Teva Pharmaceutical Industries Ltd, West Chester, Pennsylvania, USA.
Honglue ShenNonclinical Development Teva Pharmaceutical Industries Ltd, West Chester, Pennsylvania, USA.
Hussein HallakSpecialty Clinical Development, Teva Pharmaceutical Industries Ltd, Netanya, Israel.
Pippa S LoupeNonclinical Development Teva Pharmaceutical Industries Ltd, West Chester, Pennsylvania, USA.
Michael SmithDevice R&D, Teva Pharmaceutical Industries Ltd, Runcorn, United Kingdom.
Laura Rabinovich-GuilattSpecialty Clinical Development, Teva Pharmaceutical Industries Ltd, Netanya, Israel.
Ofer SpiegelsteinSpecialty Clinical Development, Teva Pharmaceutical Industries Ltd, Netanya, Israel.
Teva Pharmaceuticals (Israel) · ILTeva Pharmaceuticals (United States) · USCalifornia Miramar University · USTeva Pharmaceuticals (Czechia) · CZTeva Pharmaceuticals (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fremanezumab (AJOVY; Teva Pharmaceutical Industries Ltd, Netanya, Israel), approved for the preventive treatment of migraine, is available as a subcutaneous injection either once a month or once every 3 months using an autoinjector or a prefilled syringe. The present study evaluated the pharmacokinetic (PK) bioequivalence of a single subcutaneous injection of fremanezumab 225 mg administered using an autoinjector compared to a prefilled syringe in healthy volunteers. Blood samples for PK and antidrug antibodies were collected before and after dosing. Safety and tolerability assessments included physical examinations, adverse event reporting, laboratory evaluations, and immunogenicity. Following single-dose administration, the mean concentration-time profiles for the 2 treatment groups (autoinjector, n = 106; and prefilled syringe, n = 110) were similar. The point estimates for the back-transformed ratio (autoinjector/prefilled syringe) of geometric least squares means of maximum plasma concentration, area under the plasma concentration-time curve from time 0 to the time of the last measurable drug concentration, and area under the plasma concentration-time curve from time 0 extrapolated to infinity were 1.03, 1.04, and 1.05, respectively, with the 90% confidence intervals entirely contained within bioequivalence margins of 0.8 to 1.25. For both groups, median time to maximum observed concentration was 5 days and mean terminal elimination half-life was approximately 29 days. Treatment-related adverse events were reported by 39 (36%) subjects in the autoinjector group and 26 (24%) in the prefilled syringe group, and the majority were nonserious injection site reactions. The incidence of treatment-emergent antidrug antibody response was low and evenly distributed between the autoinjector (n = 3; 3%) and prefilled syringe (n = 4; 4%) groups. These results indicate that the fremanezumab autoinjector presentation provides an easy-to-use bioequivalent PK profile with a similar safety and tolerability profile to that of the prefilled syringe.

Indexed as

AdolescentAdultAntibodies, MonoclonalArea Under CurveCalcitonin Gene-Related PeptideEquipment DesignFemaleHalf-LifeHumansInjections, SubcutaneousMaleMiddle AgedTherapeutic EquivalencyYoung AdultAntibodies, MonoclonalCalcitonin Gene-Related Peptidefremanezumabautoinjectorbioequivalencecalcitonin-gene-related peptideCGRPfremanezumabprefilled syringe

Identifiers

PMID33411992
PMCPMC8451805
OpenAlexW3120040964

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.