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Completed Phase 2 Interventional Results available

Dose Range Finding Study of Bimagrumab in Sarcopenia

ClinicalTrials.gov ID: NCT02333331

Public ClinicalTrials.gov record NCT02333331. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 12:45 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 28 Week, Randomized, Double-blind, Placebo-controlled, Two-part, Multi-center, Parallel Group Dose Range Finding Study to Assess the Effect of Monthly Doses of Bimagrumab 70, 210, and 700 mg on Skeletal Muscle Strength and Function in Older Adults With Sarcopenia (InvestiGAIT)

Study identification

NCT ID
NCT02333331
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
217 participants

Conditions and interventions

Conditions

Interventions

  • bimagrumab Drug
  • placebo Other

Drug · Other

Eligibility (public fields only)

Age range
70 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 8, 2014
Primary completion
Jun 25, 2018
Completion
Jun 27, 2018
Last update posted
Jan 4, 2021

2014 – 2018

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Novartis Investigative Site Little Rock Arkansas 72205
Novartis Investigative Site Cypress California 90630
Novartis Investigative Site La Jolla California 92093-9405
Novartis Investigative Site Farmington Connecticut 06030-5215
Novartis Investigative Site Gainesville Florida 32611
Novartis Investigative Site Miami Florida 33143
Novartis Investigative Site Miami Lakes Florida 33014
Novartis Investigative Site Orlando Florida 32804
Novartis Investigative Site Gainesville Georgia 30501
Novartis Investigative Site Boston Massachusetts 02115
Novartis Investigative Site Rochester Minnesota 55905
Novartis Investigative Site High Point North Carolina 27262
Novartis Investigative Site Columbus Ohio 43210
Novartis Investigative Site Spartanburg South Carolina 29303
Novartis Investigative Site Mesquite Texas 75150
Novartis Investigative Site San Antonio Texas 78229
Novartis Investigative Site Madison Wisconsin 53706

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02333331, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 4, 2021 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02333331 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →