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IGF-1 LR3 clinical trials

ClinicalTrials.gov lists 9 registered trials of IGF-1 LR3: 0 recruiting or about to, 0 running, 5 completed, 4 in phase 3, 5 with results posted. The largest is IGFD Registry: A Patient Registry for Monitoring Long-term Safety and Efficacy of Increlex (1,378 people).

9registered trials

0recruiting now

0running

5completed

4in phase 3

5with results posted

Completed: 5Stopped or withdrawn: 49trials
  • Completed 5
  • Stopped or withdrawn 4

Where IGF-1 LR3 is in testing

Registered trials by phase. Phase 3 trials are the large ones that decide approval.

0Early phase 1First doses in people
1Phase 1Safety and dosing
2Phase 2Does it work?
4Phase 3Large confirmatory trials
0Phase 4After approval
2Not phasedObservational and other

Timeline

Each bar runs from a trial's start to its planned end; faded bars have no end date. Click a bar to open the trial.

199219941996199820002002200420062008201020122014201620182020202220242026Evaluation of the Safety and Efficacy of Using Insulin-like Growth Factor-1 in Patients With a Heart Attack · Completed · Phase 1, Phase 2 · 47 people · 2011-10 to 2016-02IGF-I Stimulation of Collagen Synthesis in Ehlers-Danlos Patients · Completed · No phase · 15 people · 2011-09 to 2012-11Effects of IGF-I in HIV Metabolic Disease · Stopped or withdrawn · Phase 1 · 16 people · 2011-06 to 2013-06rhGH and rhIGF-1 Combination Therapy in Children With Short Stature Associated With IGF-1 Deficiency · Stopped or withdrawn · Phase 2 · 106 people · 2007-12 to 2010-04IGFD Registry: A Patient Registry for Monitoring Long-term Safety and Efficacy of Increlex · Stopped or withdrawn · No phase · 1,378 people · 2006-06 to 2014-05Treatment of Children and Adolescents With Growth Failure Associated With Primary IGF-1 Deficiency · Stopped or withdrawn · Phase 3 · 114 people · 2005-11 to 2010-02Recombinant Human Insulin-Like Growth Factor (rhIGF-1) Treatment of Short Stature Associated With IGF-1 Deficiency · Completed · Phase 2, Phase 3 · 45 people · 2005-07 to 2009-01Prepubertal Children With Growth Failure Associated With Primary Insulin-Like Growth Factor-1 (IGF-1) Deficiency · Completed · Phase 3 · 137 people · 2004-03 to 2008-07Long-Term Treatment With rhIGF-1 in GHIS · Completed · Phase 2, Phase 3 · 92 people · 1991-05-20 to 2011-12-15
RecruitingRunningCompletedStopped or withdrawnStatus unknownToday

Completed 5

Prepubertal Children With Growth Failure Associated With Primary Insulin-Like Growth Factor-1 (IGF-1) Deficiency

CompletedPhase 3137 peopleRandomizedIpsen2004-03 → 2008-07🇺🇸 United StatesResults posted

Studying: Growth Disorders, Insulin-Like Growth Factor-1 Deficiency · NCT00125164

About this trial

This study is intended to determine whether twice daily weight based dosing with recombinant human insulin-like growth factor (rhIGF-1) will safely and effectively increase the growth of prepubertal children with short stature associated with low IGF-1 levels but who produce sufficient growth hormone (GH). Subjects will be randomized to either an observation arm or to active treatment.

Long-Term Treatment With rhIGF-1 in GHIS

CompletedPhase 2, Phase 392 peopleIpsen1991-05-20 → 2011-12-15🇺🇸 United StatesResults posted

Studying: Growth Hormone Insensitivity Syndrome · NCT00571727

About this trial

The objective of this study was to evaluate the long-term safety and effectiveness of mecasermin (the study drug) in children with growth failure due to severe Primary insulin-like growth factor-1 deficiency (Primary IGFD).

Evaluation of the Safety and Efficacy of Using Insulin-like Growth Factor-1 in Patients With a Heart Attack

CompletedPhase 1, Phase 247 peopleRandomizedUniversity College Cork2011-10 → 2016-02🇮🇪🇳🇱 Ireland, Netherlands

Studying: Heart Failure, Myocardial Infarction · NCT01438086

About this trial

When a patient has a heart attack, a blockage occurs in a coronary artery that delivers oxygen to the heart muscle. The heart muscle may weaken, causing heart failure. The body naturally makes a protein called insulin-like growth factor-1 (IGF-1) that may protect the heart muscle cells from dying and may prevent heart failure or lessen the damage that occurs. IGF-1 is also available as a drug called mecasermin. In this study, heart attack patients will be given either a dose of mecasermin or a placebo (inactive treatment) after their coronary artery has been opened by a stent. The purpose of t…

IGF-I Stimulation of Collagen Synthesis in Ehlers-Danlos Patients

Completed15 peopleRandomizedBispebjerg Hospital2011-09 → 2012-11🇩🇰 Denmark

Studying: Ehlers-Danlos Syndrome, Classic · NCT01446783

About this trial

The investigators want to inject insulin-like growth factor-I (IGF-I) into the patella tendon of Ehlers-Danlos patients and healthy controls to evaluate the response in collagen synthesis. Furthermore collagen synthesis is measured in muscle connective tissue and in skin. The hypothesis is that the connective tissue in Ehlers-Danlos patients is more compliant and poorer in collagen than healthy controls, but that collagen synthesis can be stimulated by IGF-I.

Stopped early or withdrawn 4

Effects of IGF-I in HIV Metabolic Disease

TerminatedPhase 116 peopleRandomizedUniversity of Texas Southwestern Medical Center2011-06 → 2013-06🇺🇸 United States

Studying: HIV Lipodystrophy · NCT01329744

About this trial

This study examines the effects of recombinant insulin like growth factor - I on body composition, glucose homeostasis, and lipids, in adults with HIV infection and signs of metabolic disease.

rhGH and rhIGF-1 Combination Therapy in Children With Short Stature Associated With IGF-1 Deficiency

TerminatedPhase 2106 peopleRandomizedIpsen2007-12 → 2010-04🇺🇸 United StatesResults posted

Studying: Insulin-like Growth Factor-1 Deficiency · NCT00572156

About this trial

IGF-1 (insulin-like growth factor-1) is a hormone that is normally produced in the body in response to another hormone called growth hormone. Growth Hormone is produced by a small gland at the base of the brain (the pituitary). Together IGF-1 and GH are large contributors to growth during infancy, childhood, and adolescence. Children with IGF Deficiency are short and have an imbalance in the levels of growth hormone and IGF-1 that their body produces. Their growth hormone levels are normal or even high, but IGF-1 levels do not increase normally in response to growth hormone. As a result, they…

IGFD Registry: A Patient Registry for Monitoring Long-term Safety and Efficacy of Increlex

Terminated1,378 peopleIpsen2006-06 → 2014-05🇺🇸 United States

Studying: Primary Insulin-like Growth Factor-1 Deficiency · NCT00747604

About this trial

This project is a retrospective (beginning January 2006) and prospective patient registry program sponsored by Ipsen (formerly Tercica, Inc.). In collaboration with participating health care practitioners, the patient registry program is an observational study monitoring the long-term safety of patients treated with Increlex® (mecasermin \[rDNA origin\] injection). The IGFD (Increlex® Growth Forum Database) Registry is intended primarily to monitor the safety and efficacy of Increlex replacement therapy in children with growth failure.

Treatment of Children and Adolescents With Growth Failure Associated With Primary IGF-1 Deficiency

TerminatedPhase 3114 peopleIpsen2005-11 → 2010-02🇫🇷 FranceResults posted

Studying: Growth Disorders · NCT00330668

About this trial

This is an extension study to Tercica study MS301 (NCT00125164) and is intended to collect long term safety and efficacy data on the continued use of recombinant human insulin-like growth factor-1 (rh IGF-1) in children and adolescents treated for primary IGF-1 deficiency (IGFD). The secondary objective is to use the data collected to learn more about the relationship of IGF-1 exposure to the promotion of normal growth and pubertal development.

Registered trials include ones that haven't published results yet. Trials are matched on the compound's name and code names (IGF-1 LR3, mecasermin) in the listed interventions.