Evidence map›Paper›PMID 37334968›Full record

ArticleeLife2023

Development and biophysical characterization of a humanized FSH-blocking monoclonal antibody therapeutic formulated at an ultra-high concentration.

Satish Rojekar, Anusha R Pallapati, Judit Gimenez-Roig, Funda Korkmaz, Farhath Sultana, Damini Sant, Clement M Haeck, Anne Macdonald, Se-Min Kim, Clifford J Rosen and 6 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Latest Advancements in Biotherapeutics.Current pharmaceutical biotechnology · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. FSH, bone, belly and brain.The Journal of endocrinology · 2024
    Review
  14. Article
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Satish RojekarCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.ORCID 0000-0002-3301-5941
Anusha R PallapatiCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Judit Gimenez-RoigCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Funda KorkmazCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Farhath SultanaCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Damini SantCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Clement M HaeckCenter for Biomedical Research, Population Council, New York, United States.ORCID 0000-0003-4856-1440
Anne MacdonaldCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Se-Min KimCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Clifford J RosenMaine Medical Center Research Institute, Scarborough, United States.ORCID 0000-0003-3436-8199
Orly BarakCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Marcia MeseckCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
John CaminisCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Daria LiznevaCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Tony YuenCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.
Mone ZaidiCenter for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, United States.ORCID 0000-0001-5911-9522
Icahn School of Medicine at Mount Sinai · USMaine Medical Center Research Institute · USPopulation Council · US

Funding

Targeting FSH for the Therapy of Osteoporosis, Obesity and NeurodegenerationU19AG060917 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Mone Zaidi · 2019 to 2026
$29.0M
The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI Lucy Liaw · 2017 to 2026
$25.1M
A Humanized Monoclonal FSH Blocking Antibody for Alzheimer's DiseaseU01AG073148 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Tony Yuen, Mone Zaidi · 2021 to 2026
$10.6M
Elevated FSH - A Driver for Sex Differences in Alzheimer's DiseaseR01AG074092 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAROUTUNIAN, VAHRAM, YUEN, TONY · 2021 to 2025
$6.3M
Proof-of-Concept and Mechanistic Studies to Repurpose Erectile Dysfunction Drugs for Elderly FemalesR01AG071870 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KIM, SE-MIN, YUEN, TONY · 2021 to 2025
$3.9M
Thyrotropin Receptor, Thyrotropin and Mechanisms of Bone LossR01DK113627 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DAVIES, TERRY FRANCIS, IQBAL, JAMEEL Z · 2017 to 2020
$2.8M
NIA NIH HHS R01 AG071870NIA NIH HHS R01 AG074092NIA NIH HHS U01 AG073148NIA NIH HHS U01AG073148NIA NIH HHS U19 AG060917NIDDK NIH HHS R01 DK113627NIGMS NIH HHS P20 GM121301
6 · The paper itself

Abstract

Highly concentrated antibody formulations are oftentimes required for subcutaneous, self-administered biologics. Here, we report the development of a unique formulation for our first-in-class FSH-blocking humanized antibody, MS-Hu6, which we propose to move to the clinic for osteoporosis, obesity, and Alzheimer's disease. The studies were carried out using our Good Laboratory Practice (GLP) platform, compliant with the Code of Federal Regulations (Title 21, Part 58). We first used protein thermal shift, size exclusion chromatography, and dynamic light scattering to examine MS-Hu6 concentrations between 1 and 100 mg/mL. We found that thermal, monomeric, and colloidal stability of formulated MS-Hu6 was maintained at a concentration of 100 mg/mL. The addition of the antioxidant L-methionine and chelating agent disodium EDTA improved the formulation's long-term colloidal and thermal stability. Thermal stability was further confirmed by Nano differential scanning calorimetry (DSC). Physiochemical properties of formulated MS-Hu6, including viscosity, turbidity, and clarity, confirmed with acceptable industry standards. That the structural integrity of MS-Hu6 in formulation was maintained was proven through Circular Dichroism (CD) and Fourier Transform Infrared (FTIR) Spectroscopy. Three rapid freeze-thaw cycles at -80 °C/25 °C or -80 °C/37 °C further revealed excellent thermal and colloidal stability. Furthermore, formulated MS-Hu6, particularly its Fab domain, displayed thermal and monomeric storage stability for more than 90 days at 4°C and 25°C. Finally, the unfolding temperature (T

Indexed as

Antibodies, MonoclonalFollicle Stimulating HormoneCalorimetry, Differential ScanningProtein StabilityTemperatureViscosityAntibodies, MonoclonalFollicle Stimulating Hormoneaccelerated stabilitybiologicsbiotherapeuticsdifferential fluorescence spectroscopydrug developmentexcipient screeningmedicinemonoclonal antibodynone

Identifiers

PMID37334968
PMCPMC10325703
OpenAlexW4381191076

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.