Skip to content

Trial · Interventional

CompletedPhase 2Results postedRegistry data

Effect of GLP-1 Analogue ROSE-010 on Appetite in Overweight and Obese Subjects

This trial does not test a peptide that PepBank tracks.

  • Measures Glucagon, does not give it. It appears in the eligibility rules.

Overview

Status
Completed
Phase
Phase 2
Enrollment
40 participants (actual)
Sponsor
Rose Pharma Inc · Industry
Design
Randomized · Quadruple masking
Countries
1 country

United States

Start
26 Sept 2024
Primary completion
27 Feb 2025
Completion
27 Feb 2025
First posted
1 Oct 2024
Last update posted
1 Jun 2026
Conditions
Obesity; Overweight

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
202420252026
  1. Ph 2

    Effect of GLP-1 Analogue ROSE-010 on Appetite in Overweight and Obese Subjects

    NCT06621017

    26 Sept 2024 to 27 Feb 2025

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The primary objective of this study is to assess the efficacy of ROSE-010 on food intake in female subjects with overweight and obesity. The secondary objectives of this study are the following: * To assess the efficacy of ROSE-010 on hunger; * To assess the efficacy of ROSE-010 on satiety; * To assess the efficacy of ROSE-010 on prospective consumption; * To assess the efficacy of ROSE-010 on desire to eat; * To assess the efficacy of ROSE-010 on palatability; * To characterize the pharmacokinetics (PK) of ROSE-010 following subcutaneous (SC) administration on Day 1 and Day 7; and * To evaluate safety and tolerability of SC administrations of ROSE-010 to overweight and obese subjects.

Interventions

  • ROSE-010 99 mcgDrug
  • PlaceboDrug
  • ROSE-010 150 mcgDrug

Arms3

  • Placebo comparator

    Placebo

    Saline solution

  • Experimental

    ROSE-010 99 mcg

    ROSE-010 solution, 99 mcg, 0.5 ml

  • Experimental

    ROSE-010 150 mcg

    ROSE-010 solution, 150 mcg, 0.5 ml

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Food Consumption

    Time frame · 30 minutes

    Registry description

    The amount of food (weight and energy content) consumed during lunch after administration of ROSE-010 at 2 dose levels compared to placebo.

Secondary outcomes(9)
  1. Hunger

    Time frame · 6.5 hours Day 7

    Registry description

    Hunger across 6.5 hours of Area Under Evaluation (AUE) defined by time in hours (h) multiplied by the subject reported value on a visual analogue scale at each time point measured in mm on a 0 to 100 mm scale and where 0 is not hungry at all and 100 is maximum hunger. AUE is a sum of hunger across the time period and is calculated as h\*mm. Simplistically, if the subject was not hungry at all across the period the AUE would be zero. The higher the AUE number, the higher the level of hunger throughout the observation period.

  2. Satiety

    Time frame · 6.5 hours Day 7

    Registry description

    Satiety across 6.5 hours of Area Under Evaluation (AUE) defined by time in hours (h) multiplied by the subject reported value on a visual analogue scale at each time point measured in mm on a 0 to 100 mm scale and where 0 is not feeling full at at all and 100 is maximum feeling of fullness. AUE is a sum of satiety across the time period and is calculated as h\*mm. Simplistically, if the subject was not full at all across the period the AUE would be zero. The higher the AUE number, the higher the level of satiety throughout the observation period.

  3. Prospective Consumption

    Time frame · 6.5 hours Day 7

    Registry description

    Prospective consumption across 6.5 hours of Area Under Evaluation (AUE) defined by time in hours (h) multiplied by the subject reported value on a visual analogue scale at each time point measured in mm on a 0 to 100 mm scale and where 0 is indicates no anticipated need to eat and 100 is maximum anticipated need to eat. AUE is a sum of prospective consumption across the time period and is calculated as h\*mm. Simplistically, if the subject has no anticipated need or desire to eat at all across the period the AUE would be zero. The higher the AUE number, the higher the level of prospective consumption throughout the observation period.

  4. Desire to Eat

    Time frame · 6.5 hours Day 7

    Registry description

    Desire to eat across 6.5 hours of Area Under Evaluation (AUE) defined by time in hours (h) multiplied by the subject reported value on a visual analogue scale at each time point measured in mm on a 0 to 100 mm scale and where 0 is no desire to eat at all and 100 is maximum desire to eat. AUE is a sum of the desire to eat across the time period and is calculated as h\*mm. Simplistically, if the subject had no desire to eat at all across the period the AUE would be zero. The higher the AUE number, the higher the desire to eat throughout the observation period.

  5. Palatability

    Time frame · 30 minutes Day 7

    Registry description

    Palatability (tastiness) score on a visual analogue scale (0 to 100 mm) where 0 is not palatable at all and 100 is the maximum palatibility. The higher the score, the more palatable the reported outcome.

  6. Nausea

    Time frame · 6.5 hours Day 7

    Registry description

    Nausea across 6.5 hours of Area Under Evaluation (AUE) defined by time in hours (h) multiplied by the subject reported value on a visual analogue scale at each time point measured in mm on a 0 to 100 mm scale and where 0 is not nauseous at all and 100 is maximum nausea. AUE is a sum of hunger across the time period and is calculated as h\*mm. Simplistically, if the subject was not nauseous at all across the period, the AUE would be zero. The higher the AUE number, the higher the level of nausea throughout the observation period.

  7. Plasma PK Analysis of ROSE-010 Time to Max Concentration Tmax

    Time frame · Day 7

    Registry description

    Plasma PK analysis of ROSE-010: Time to max plasma concentration in minutes

  8. Plasma PK Analysis of ROSE-010 Cmax

    Time frame · Day 7

    Registry description

    Plasma PK analysis of ROSE-010, measurement of max plasma concentration.

  9. Half-life

    Time frame · Day 7

    Registry description

    Time of plasma elimination half-life calculated for both ROSE-010 doses

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeLeast squares mean· 30 minutes

Food Consumption

GroupValue (weight food eaten g)Spread
Placebo605.50
ROSE-010 99 mcg404.380.55
ROSE-010 150 mcg423.679.43
Secondary and other outcome results(7)
Secondary outcomeMean· 6.5 hours Day 7

Hunger

GroupValue (AUE defined as h*mm)
Placebo220.5
ROSE-010 99 mcg212.5
ROSE-010 150 mcg177.1
Secondary outcomeMean· 6.5 hours Day 7

Satiety

GroupValue (AUE defined as h*mm)
Placebo340.3
ROSE-010 99 mcg328.1
ROSE-010 150 mcg286.6
Secondary outcomeMean· 6.5 hours Day 7

Prospective Consumption

GroupValue (AUE defined as h*mm)
Placebo247.6
ROSE-010 99 mcg227.2
ROSE-010 150 mcg183.6
Secondary outcomeMean· 6.5 hours Day 7

Desire to Eat

GroupValue (AUE defined as h*mm)
Placebo223.6
ROSE-010 99 mcg219.8
ROSE-010 150 mcg166.0
Secondary outcomeMean· 30 minutes Day 7

Palatability

GroupValue (Scores on VAS scale)
Placebo74.4
ROSE-010 99 mcg55.9
ROSE-010 150 mcg58.4
Secondary outcomeMean· 6.5 hours Day 7

Nausea

GroupValue (AUE defined as h*mm)
Placebo0.0
ROSE-010 99 mcg0.17
ROSE-010 150 mcg3.38
Secondary outcomeMedian· Day 7

Plasma PK Analysis of ROSE-010 Time to Max Concentration Tmax

GroupValue (Minutes)
Placebonot posted
ROSE-010 99 mcg26
ROSE-010 150 mcg26

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
PlaceboSaline solution0 / 100 / 103 / 10
ROSE-010 99 mcgROSE-010 solution, 99 mcg, 0.5 ml0 / 150 / 1512 / 15
ROSE-010 150 mcgROSE-010 solution, 150 mcg, 0.5 ml0 / 150 / 159 / 15

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
Female
Age
from 18 Years up to 65 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: 1. Body mass index greater or equal to 27 and less than nor equal to 35 kg/m2 at Screening. 2. Good health, as assessed by the Investigator, based on medical, surgical, and psychiatric history, physical examination, 12-lead electrocardiogram (ECG), vital sign assessments, and clinical laboratory evaluations at Screening and Check-In. 3. Subjects must have a negative serum pregnancy test result at Screening and at Check-In and must not be pregnant, lactating, or planning a pregnancy from the Screening Visit to 30 days after the last dose of study drug. 4. Female subjects of non-childbearing potential must be either surgically sterile (ie, had a hysterectomy, bilateral tubal ligation, bilateral salpingectomy, and/or bilateral oophorectomy at least 26 weeks prior to Screening) or postmenopausal (ie, have experienced spontaneous amenorrhea for at least 2 years, with a follicle-stimulating hormone level in the postmenopausal range at Screening based on the central laboratory's ranges). 5. Subjects of childbearing potential (ie, ovulating, premenopausal, and not permanently surgically sterile) with male partners will be included if they are either sexually inactive (complete abstinence from heterosexual activity if in line with the subject's preferred and usual lifestyle) for at least 30 days prior to the first dose of study drug and agree to continue complete abstinence for at least 30 days after the last administration of study drug, or, if sexually active, agree to use a medically accepted contraceptive regimen during their participation in the study and for at least 30 days after the last administration of study drug. Exclusion Criteria: 1. Clinically significant or active gastric emptying abnormality (eg, gastroparesis or gastric outlet obstruction, intestinal obstruction, or any gastrointestinal \[GI\] motility disorders); malabsorption, including chronic constipation/diarrhea, celiac disease, inflammatory bowel disease, or bowel resection; or chronic use of drugs that directly affect GI motility (eg, anticholinergics, 5-hydroxytryptamine \[serotonin\] antagonists, opiates). 2. Obesity induced by other endocrinologic disorders (eg, Cushing syndrome, acromegaly, inadequately treated hypothyroidism) or diagnosed monogenic or syndromic forms of obesity (eg, melanocortin 4 receptor deficiency or Prader-Willi syndrome). 3. Thyroid disease that is not controlled (thyroid-stimulating hormone outside normal range at Screening). 4. Symptomatic gallbladder disease within the past 2 years or history of cholecystectomy. 5. History or presence of chronic pancreatitis or presence of acute pancreatitis within 6 months before Screening. 6. A history of Major Depressive Disorder within the last 2 years. 7. Any lifetime history of a suicide attempt. 8. Previous bariatric surgery, procedure for obesity, or GI surgery altering GI passage, motility, and/or nutrient absorption or recent (within 6 months of Screening) changes in body weight (greater or equal to 5%) due to dieting, including commercial weight loss programs, or pharmacologic treatment. 9. Currently on or planning to participate in any weight loss regimen during the course of the study. 10. Personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2. 11. History of malignancy, except the following: curatively resected basal cell or squamous cell skin cancers, cervical cancer in situ, or resected colorectal polyps more than 5 years prior to Screening. 12. Abnormal fasting blood glucose (ie, greater than 125 mg/dL) at Screening or Check-In and/or HbA1c (greater than 6.4%) at Screening, or prior history/diagnosis of any type of diabetes mellitus (eg, type 1, type 2, or gestational). 13. Use of any prescribed or over-the-counter (OTC) medication other than approved contraceptives within 14 days or 5 half-lives (whichever is longer) prior to dosing on Day 1 and throughout the study. Note: Following study drug administration, medications used for the treatment of adverse events (AEs) may be allowed at the discretion of the Investigator or designee. 14. Any glucagon-like peptide-1 (GLP-1) receptor agonist, GLP-1/glucose-dependent insulinotropic polypeptide dual agonist (eg, tirzepatide), or any prescription or OTC medications intended for weight loss or with a potential impact on weight and appetite regulation (eg, stimulant medications) within 6 months of Screening. 15. Known allergy to any ingredient of ROSE-010 or any history of severe allergic reaction (including drugs, food, insect bites, or environmental allergens).

PepBank is a research reference. Talk to a doctor before you use any peptide.