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Frailty is a geriatric syndrome leading to physical deterioration including muscle wasting (sarcopenia) and unintentional weight loss. There are currently no approved therapies for frailty. Ghrelin is a hormone produced by the stomach that stimulates appetite centers in the brain. The purpose of this study is to determine the optimal subcutaneous ghrelin dose as a potential intervention for frail elderly individuals. We will examine food intake and metabolic parameters after placebo and ghrelin administration at three escalating subcutaneously administered doses.
This study is to determine the optimal ghrelin dose for use in a daily subcutaneous dosing study in frail individuals. Using data from our previous study and the published literature, we have designed a single blind, single dose administration study in which we will examine food intake after ghrelin administration and metabolic parameters (plasma glucose, insulin, free fatty acids, and cortisol) pre and post ghrelin administration.We have selected a dose range using our own and previously published studies from which we will determine subcutaneous doses to use in subsequent studies. The selection criteria for subsequent studies will be the dose that maximizes food intake by more than 30% without inducing hyperglycemia or raising cortisol levels. Participants must meet all inclusion criteria and have no exclusion criteria. Data will be analyzed after the first three participants have completed the protocol and used to inform dose modifications for the next three participants. Data from this portion of the study will be analyzed immediately after its completion, to allow updates to the design of the next study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ghrelin Group 1 | Experimental | Dose finding with each of the first two participant coming to the CTRC for four visits greater than or equal to 72 hours apart and on each receiving subcutaneous injection of - placebo (first visit) and three escalating doses of ghrelin 2ug/kg (second visit) , 5 ug/kg (third visit), and 10 ug/kg (fourth visit). |
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| Ghrelin Group 2 | Experimental | Dose finding with each of the final three participant coming to the CTRC for four visits greater than or equal to 72 hours apart and on each receiving subcutaneous injection of - placebo (first visit) and three escalating doses of ghrelin 5ug/kg (second visit) , 7.5 ug/kg (third visit), and 10 ug/kg (fourth visit). |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ghrelin Group 1 | Drug | The first two participants received placebo at baseline visit, 2 mcg/kg as a single subcutaneous dose at Visit 2, 5 mcg/kg as a single subcutaneous dose at Visit 3, and 10 mcg/Kg as a single subcutaneous dose at visit 4. There was 3-10 days between visits. |
| Measure | Description | Time Frame |
|---|---|---|
| Treatment Emergent Adverse Events | Number and type of treatment emergent adverse events | 30 days following the last administration of study treatment. |
| Median Energy Intake | Median energy intake at breakfast, which was served 30 minutes post-placebo or ghrelin administration demonstrated at each dose level. | 30 mins post-ghrelin or placebo |
| Percentage of Total Energy Intake Relative to Placebo | % of total energy relative to placebo - breakfast served 30 minutes post-placebo or ghrelin administration. | 30 mins post-ghrelin or placebo |
| Growth Hormone | median growth hormone peak 30 minutes after placebo/ghrelin. | 30 minutes after ghrelin administration |
| Cortisol Level | Cortisol response to ghrelin or placebo - levels at 0, 60 and 120 minutes after dosing | 0, 60 and 120 minutes after dosing |
| Glucose Levels | Median fasting and peak postprandial Glucose levels (60 or 90 minutes from dosing) at placebo and at each ghrelin dose. | 0 minutes (baseline) and 60 or 90 minutes from dosing |
| Insulin Level | Median fasting insulin levels at baseline and 90 minutes after dosing | 0 and 90 minutes after dosing |
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Inclusion Criteria:
Exhaustion: Two statements are read:
I felt that everything I did was an effort
I could not get going. The question is asked "How often in the last week did you feel this way?" 0 = rarely or none of the time (<1 day), 1 = some or a little of the time (1-2 days), 2 = a moderate amount of the time (3-4 days), or 3 = most of the time. A "2" or "3" response to either question is a positive response.
Exclusion Criteria:
Diabetes mellitus or fasting glucose ≥ 126 mg/dL
Hospitalization for stroke, myocardial infarction, coronary artery bypass graft surgery, vascular surgery in the past six months.
NYHA Class III or IV congestive heart failure
Therapy for cancer in the past 12 months, except non-melanoma skin cancer
BMI≥ 30 kg/m2
Current use of corticosteroids other than topical, ophthalmic, and inhaled preparations
Therapy with megestrol acetate or dronabinol within the last 6 weeks
TSH measured as <0.4 mU/L or greater than 10mU/L
Abnormal liver function tests (LFTs > 2x upper limit of normal)
Hemoglobin < 11g/dL
Insulin-like growth factor-I (IGF-I) above the age-specific reference range
History of surgery within the last 30 days
Unstable medical or psychological conditions or unstable home or food environment
Cognitive deficit as defined by a Folstein Mini Mental State Exam score < 18/30
Depression (defined as a score of >11 on the Geriatric Depression Questionnaire)
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| Name | Affiliation | Role |
|---|---|---|
| Anne R. Cappola, M.D., Sc.M. | University Of Pennsylvania, Perelman School of Medicine, Department of Endocrinology, Diabetes and Metabolism | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clinical and Translational Research Center, University of Pennsylvania | Philadelphia | Pennsylvania | 19104 | United States |
Dose finding with each participant receiving placebo at their first study visits and three escalating doses of ghrelin, separated by 3-7 days in visits 2,3 and 4.
Study participants were recruited from community dwelling adults meeting study criteria expressing interest in participating in research studies at University of Pennsylvania.
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| ID | Title | Description |
|---|---|---|
| FG000 | Initial Dosing Group | Visit 1: Placebo Visit 2: 2 ug/kg ghrelin Visit 3: 5 ug/kg ghrelin Visit 4: 10 ug/kg ghrelin |
| FG001 | Second Dosing Group | Visit 1: Placebo Visit 2: 5 ug/kg ghrelin Visit 3: 7.5 ug/kg ghrelin Visit 4: 10 ug/kg ghrelin |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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| ID | Title | Description |
|---|---|---|
| BG000 | Ghrelin | Dose finding with each participant receiving placebo and three doses of ghrelin, separated by 3-7 days Ghrelin: The first three participants will receive 2 mcg/kg as a single subcutaneous dose at Visit 3, 5 mcg/kg as a single subcutaneous dose at Visit 4, and 10 mcg/Kg as a single subcutaneous dose at visit 5. There will be 3-10 days between visits. The next three participants will receive either the same dosing at the first three, a regimen that includes an intermediate dose (e.g., 7.5 mcg/kg), or higher (e.g., 12, 15, and 18 mcg/kg) doses. |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Treatment Emergent Adverse Events | Number and type of treatment emergent adverse events | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2,3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Number | Events | 30 days following the last administration of study treatment. |
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Recorded from study screen through 30 days after the final study visit. Assessed systematically during study visits at time 0, 15, 30, 45, 60, 90 120, and 150 minutes after dosing and 1 day after all study visits by telephone call to subject.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Placebo | Visit 1 for all five subjects placebo injected s.c. at time 0 |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| bristley feeling in chest | General disorders | Systematic Assessment | reported day after placebo visit, occurred and resolved in one minute with no action. |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Anne Cappola, PI | University of Pennsylvania | 215-573-5359 | acappola@mail.med.upenn.edu |
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| Ghrelin Group 2 | Drug | The next three participants received placebo at baseline visit, 5 mcg/kg as a single subcutaneous dose at Visit 2, 7.5 mcg/kg as a single subcutaneous dose at Visit 3, and 10 mcg/Kg as a single subcutaneous dose at visit 4. |
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| Free Fatty Acid Level | Free Fatty Acid levels (mEq/L) at 60 and 90 minutes after meal (90 and 120 minutes) | 90 and 120 minutes after dosing |
| years |
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| Sex: Female, Male | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
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| OG002 | 5ug/kg | The first two participants received 5ug/kg of s.c. ghrelin at visit 3. The final three participants received 5ug/kg of s.c. ghrelin at visits 2. |
| OG003 | 7.5ug/kg | The final three participants received 7.5ug/kg of s.c. ghrelin at visit 3. |
| OG004 | 10ug/kg | The first two participants received 10ug/kg of s.c. ghrelin at visit 4. The final three participants received 10ug/kg of s.c. ghrelin at visit 4. |
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| Primary | Median Energy Intake | Median energy intake at breakfast, which was served 30 minutes post-placebo or ghrelin administration demonstrated at each dose level. | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2, 3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Median | Full Range | Kilocalories | 30 mins post-ghrelin or placebo |
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| Primary | Percentage of Total Energy Intake Relative to Placebo | % of total energy relative to placebo - breakfast served 30 minutes post-placebo or ghrelin administration. | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2,3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Number | percentage of placebo intake | 30 mins post-ghrelin or placebo |
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| Primary | Growth Hormone | median growth hormone peak 30 minutes after placebo/ghrelin. | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2,3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Median | Full Range | ng/mL | 30 minutes after ghrelin administration |
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| Primary | Cortisol Level | Cortisol response to ghrelin or placebo - levels at 0, 60 and 120 minutes after dosing | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2,3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Median | Full Range | mcg/dL | 0, 60 and 120 minutes after dosing |
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| Primary | Glucose Levels | Median fasting and peak postprandial Glucose levels (60 or 90 minutes from dosing) at placebo and at each ghrelin dose. | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2,3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Median | Full Range | mg/dL | 0 minutes (baseline) and 60 or 90 minutes from dosing |
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| Primary | Insulin Level | Median fasting insulin levels at baseline and 90 minutes after dosing | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2,3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Median | Full Range | uIU/mL | 0 and 90 minutes after dosing |
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| Primary | Free Fatty Acid Level | Free Fatty Acid levels (mEq/L) at 60 and 90 minutes after meal (90 and 120 minutes) | At the first visit all participants received s.c. placebo. The first two participants received 2 ,5, and 10ug/kg of ghrelin at visit 2,3 and 4 consecutively. The final three participants received 5,7.5, and 10ug/kg of s.c. ghrelin at visits 2,3 and 4 consecutively. | Posted | Median | Full Range | mEq/L | 90 and 120 minutes after dosing |
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| 0 |
| 5 |
| 2 |
| 5 |
| EG001 | 2mcg/kg | Visit 2 for the first two subjects 2mcg/kg ghrelin injected s.c at time 0 | 0 | 2 | 0 | 2 |
| EG002 | 5mcg/kg | Visit 3 for the first two subjects Visit 2 for the last three subjects 5mcg/kg ghrelin injected s.c. at time 0 | 0 | 5 | 1 | 5 |
| EG003 | 7.5mcg/kg | Visit 3 for the last three subjects 7.5mcg/kg ghrelin injected at time 0 | 0 | 3 | 3 | 3 |
| EG004 | 10mcg/kg | Visit 4 for all five subjects | 0 | 5 | 1 | 5 |
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| awareness of sternotomy incision | Skin and subcutaneous tissue disorders | Systematic Assessment | occurred during visit 30 minutes after ghrelin administration and resolved within 15 minutes with no action. |
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| dizziness | Nervous system disorders | Systematic Assessment | "dizzy is too strong - woozy" |
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| burping | Gastrointestinal disorders | Systematic Assessment | during study visit 15 minutes after meal completion |
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| warmth | General disorders | Systematic Assessment | passing sensation between 45 and 60 minutes from ghrelin injection resolving with no action |
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| euphoria | General disorders | Systematic Assessment | passing feeling during study visit 1 hour after ghrelin administration |
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| 60 minutes after dosing |
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| 120 minutes after dosing |
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| peak postprandial (60 or 90 minutes after dosing) |
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| 90 minutes after dosing |
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| 120 minutes |
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