MedPath

Pegvisomant

Generic Name
Pegvisomant
Brand Names
Somavert
Drug Type
Biotech
CAS Number
218620-50-9
Unique Ingredient Identifier
N824AOU5XV
Background

Pegvisomant is a highly selective growth hormone (GH) receptor antagonist. It is used to treat acromegaly. Unlike dopamine or somatostatin analogs (which inhibit growth hormone secretion), this drug actually blocks the hepatic (GH-mediated) production of insulin like growth factor (IGF-1), which is the main mediator of growth hormone activity.

Indication

Pegvisomant is a growth hormone receptor antagonist used for the treatment of acromegaly.

Associated Conditions
Acromegaly

Effect of DPP4 Inhibition on Growth Hormone Secretion

Phase 4
Completed
Conditions
Obesity
Interventions
First Posted Date
2012-10-05
Last Posted Date
2018-05-29
Lead Sponsor
Vanderbilt University
Target Recruit Count
44
Registration Number
NCT01701973
Locations
🇺🇸

Vanderbilt University Medical Center, Nashville, Tennessee, United States

Acromegaly Combination Treatment Study

Not Applicable
Terminated
Conditions
Acromegaly
Interventions
First Posted Date
2012-02-27
Last Posted Date
2023-01-04
Lead Sponsor
Cedars-Sinai Medical Center
Target Recruit Count
76
Registration Number
NCT01538966
Locations
🇺🇸

Cedars-Sinai Medical Center, Los Angeles, California, United States

Study to Evaluate the Efficacy and Safety of Sandostatin LAR at High Dose or in Combination Either With GH-receptor Antagonist or Dopamine-agonist in Acromegalic Patients

Phase 4
Completed
Conditions
Acromegaly
Interventions
First Posted Date
2011-01-17
Last Posted Date
2017-03-03
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
70
Registration Number
NCT01278342
Locations
🇮🇹

Novarts Investigative Site, Naples, Italy

🇨🇭

Novartis Investigative Site, Lausanne, Switzerland

Tissue Biomarker for Pegvisomant Action

Not Applicable
Completed
Conditions
Acromegaly
Interventions
First Posted Date
2010-12-16
Last Posted Date
2017-08-22
Lead Sponsor
Cedars-Sinai Medical Center
Target Recruit Count
8
Registration Number
NCT01261000
Locations
🇺🇸

Cedars-Sinai Medical Center, Los Angeles, California, United States

Safety, Tolerability and Relative Bioavailability of Pegvisomant in Healthy Subjects

Phase 1
Completed
Conditions
Bioavailability
Interventions
First Posted Date
2010-08-13
Last Posted Date
2012-01-05
Lead Sponsor
Pfizer
Target Recruit Count
14
Registration Number
NCT01181973
Locations
🇸🇬

Pfizer Investigational Site, Singapore, Singapore

Figitumumab Combined With Pegvisomant For Advanced Solid Tumors

Phase 1
Terminated
Conditions
Colorectal Neoplasms
Lung Neoplasms
Breast Neoplasms
Prostatic Neoplasms
Sarcoma
Interventions
First Posted Date
2009-09-14
Last Posted Date
2013-12-13
Lead Sponsor
Pfizer
Target Recruit Count
24
Registration Number
NCT00976508
Locations
🇩🇪

Pfizer Investigational Site, Muenster, Germany

The Relationship Between the Growth Hormone (GH)- Insulin Like Growth Factor I (IGF-I) System and the Inflammatory System in Healthy Normal Persons

Not Applicable
Conditions
Interaction Between the GH/IGF-I System and the Immune-system
Interventions
First Posted Date
2009-09-01
Last Posted Date
2009-09-01
Lead Sponsor
Herlev Hospital
Target Recruit Count
12
Registration Number
NCT00969644
Locations
🇩🇰

Department of Endocrinology J 106, Herlev Hospital, Herlev, Denmark

Long Term Use of Somavert (Pegvisomant) For A Regulatory Post Marketing Commitment Plan

Completed
Conditions
Acromegaly
Interventions
First Posted Date
2008-04-15
Last Posted Date
2023-09-25
Lead Sponsor
Pfizer
Target Recruit Count
251
Registration Number
NCT00658879

Co-treatment With Pegvisomant and a Somatostatin Analogue (SA) in SA-responsive Acromegalic Patients

Not Applicable
Completed
Conditions
Acromegaly
Insulin Resistance
Impaired Glucose Tolerance
Interventions
First Posted Date
2008-04-03
Last Posted Date
2012-01-26
Lead Sponsor
University of Aarhus
Target Recruit Count
18
Registration Number
NCT00652379
Locations
🇩🇰

Department of Endocrinology, Aarhus University Hospital, Aarhus C, Aarhus, Denmark

Change in Quality of Life After Addition of Weekly 40 mg Pegvisomant/Placebo in Controlled Acromegalic Patients

Phase 4
Completed
Conditions
Quality of Life
Acromegaly
Interventions
First Posted Date
2008-03-25
Last Posted Date
2008-03-25
Lead Sponsor
Erasmus Medical Center
Target Recruit Count
20
Registration Number
NCT00642720
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