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Trial record 75 of 82668 for:    subjects

Non-inferiority Evaluation of Pain Intensity After Biomatrop (Somatropin) Application in Relation to Hormotrop (Somatropin), in Healthy Subjects

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ClinicalTrials.gov Identifier: NCT03634514
Recruitment Status : Not yet recruiting
First Posted : August 16, 2018
Last Update Posted : August 17, 2018
Sponsor:
Information provided by (Responsible Party):
Ache Laboratorios Farmaceuticos S.A.

Brief Summary:
Randomized, Double-blind, Controlled, Crossover, in which 68 subjects (34 males and 34 females) will receive, in each stage, an application of 4 UI, subcutaneous, single dose, of the investigational drug (Recombinant Human Somatropin - Biomatrop) and the comparator (Recombinant Human Somatropin - Hormotrop) according to randomization to evaluate the Non-inferiority of Pain Intensity After the Application of Hormotrop, using Visual Analogue Scale (0-10cm) and record the incidence of adverse events.

Condition or disease Intervention/treatment Phase
Healthy Subjects Drug: Recombinant human growth hormone - Biomatrop Drug: Recombinant human growth hormone - Hormotrop Phase 4

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 68 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Supportive Care
Official Title: National, Monocentric, Randomized, Double-blind, Controlled, Crossover Clinical Trial, to Evaluate the Non-inferiority of Pain Intensity After the Application of Recombinant Human Somatropin - Biomatrop (Biosintética Farmacêutica) in Relation to Recombinant Human Somatotropin - Hormotrop (Bergamo), Single Dose, in Healthy Subjects of Both Genders
Estimated Study Start Date : August 27, 2018
Estimated Primary Completion Date : September 2018
Estimated Study Completion Date : October 2018

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Application of Biomatrop
A single dose of Recombinant Human Somatropin - Biomatrop is administered. The pain intensity is evaluated using visual analogue scale (0-10cm) and record the incidence of adverse events.
Drug: Recombinant human growth hormone - Biomatrop
The subjects who recieve Biomatrop first, after a period maximum of 24 hours will recieve a dose of Hormotrop.

Drug: Recombinant human growth hormone - Hormotrop
The subjects who recieve Hormotrop first, after a period maximum of 24 hours will recieve a dose of Biomatrop.

Active Comparator: Application of Hormotrop
A single dose of Recombinant Human Somatropin - Hormotrop is administered. The pain intensity is evaluated using visual analogue scale (0-10cm) and record the incidence of adverse events.
Drug: Recombinant human growth hormone - Biomatrop
The subjects who recieve Biomatrop first, after a period maximum of 24 hours will recieve a dose of Hormotrop.

Drug: Recombinant human growth hormone - Hormotrop
The subjects who recieve Hormotrop first, after a period maximum of 24 hours will recieve a dose of Biomatrop.




Primary Outcome Measures :
  1. Pain Intensity [ Time Frame: 1 hour ]
    Report the Pain Intensity using Visual Analogue Scale (0-10cm)



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Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Skin phototype from 2 to 4, according to Fitspatrick classification: http://www.sbd.org.br/dermatologia/pele/cuidados/classifica cao-dos-fototipos-de-pele/ ;
  • Subjects with normal laboratory, type 1 urine exam, vital signs and ECG results;
  • Weight ≥ 50kg and Body Mass Index ≤ 30 ;
  • Healthy subject according with clinical history
  • Ability to understand and consent their participation in this clinical study, expressed by signing the Informed Consent Form (ICF);
  • Subject who have negative results for stool protoparasitological examination accomplished in clinical study. Subjects with positive results for Endolimax nana, Entamoeba hartmanni, Entamoeba coli, Iodamoeva btshlii, Chilomastix mesili, Trichomonas hominis, Retortamonas intestinalis e Enteromonas hominis will be able to be included in the study. At the end of the study those subjects will be guided to treatment according to clinic investigator criteria.

Exclusion Criteria:

  • Laboratory and clinical exam results out of normal range values, unless considered by physician clinically irrelevant;
  • Positive sorology for HIV;
  • Positive sorology for Hepatitis B;
  • Positive sorology for Hepatitis C;
  • Known hypersensitivity to the components of the medicines used during the study or related chemical compounds;
  • Subjects that has participated in clinical trial protocols in the last twelve (12) months (National Board of Health- Resolution 251 of 07 August 1997, Part III, sub-item J), unless the investigator considers that there may be a direct benefit to it;
  • Use of any type of regular medication within two (2) weeks or five (5) half-lives (whichever lasts longer) before administration of the first dose of the investigational product (IP). The eventual use of medication, which in the opinion of the Principal Investigator or physician does not interfere with the pharmacokinetics of IP in study will not be considered as exclusion criteria;
  • History of alcohol abuse or having ingested alcoholic drink 24 hours prior to IP administration;
  • History of psychotropic drug use and / or positive outcome for any of the components of the drug abuse test for amphetamine, benzoylecgonine (cocaine), benzodiazepines, methamphetamine, opiates, morphine, etrahydrocannabinol-THC (Marijuana / Marijuana). Subjects who used marijuana and hashish in less than three months before the consultation will be excluded. For drugs like cocaine, crack and heroin will be excluded subjects who present any use history;
  • Any finding of clinical observation, laboratory abnormality or therapy which, in the opinion of the investigator, may put the subject at risk or interfere with the purpose of the study;
  • The subject have any condition that in investigator's opinion prevents him/her from participating in the study;
  • History of food allergy or hyperactivity to medications or food;
  • Regular smokers or ex-smokers who have stopped for less than 6 months;
  • Subjects who have a relationship of kinship to second degree or any bond with the sponsor or research center employees;
  • Subjects with the following ECG changes: sinus tachycardia with heart rate ˃ 120 bpm; bradycardia sinus heart rate <50 bpm; atrial tachycardia, ventricular or junctional; ectopic atrial rhythm; atrial fibrillation; atrial flutter; accelerated idioventricular rhythm; locking atrium ventricular (BAV) of 1º, 2º and 3º degrees; ventricular pre-excitation; complete blockage of right or left branch; rhythm of pacemaker; supraventricular tachycardia (nodal tachycardia, ventricular atrial tachycardia) or any other clinically significant;
  • Male subjects who do not agree to use acceptable contraceptive methods: (a) contraceptive methods for the participant: barrier preservative, except for (vasectomy) or for participants who declare that they do not engage in sexual practices or exercise them non-reprodutively; (b) contraceptive methods for the partner: oral contraceptive, intravenous contraceptive, intrauterine device (IUD), hormonal implant, hormonal transdermal patch, tubal ligation, and barrier methods except for female partners that are surgically sterile (bilateral oophorectomy or hysterectomy), or menopause for at least 01 (one) year;
  • Women who do not agree to use acceptable contraceptive methods (oral contraceptive, intravenous contraceptive, intrauterine device (IUD), hormonal implant, barrier methods, hormonal transdermal patch and tubal ligation); except for those surgically sterile (bilateral oophorectomy or hysterectomy), menopause for at least one year, and participants who report not engaging in sexual practices or non-reproductive practices;
  • Women in pregnancy or nursing period.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03634514


Contacts
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Contact: Elisangela Rorato +55 11 2608-6130 Elisangela.rorato@ache.com.br

Locations
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Brazil
Instituto de Ciências Farmacêuticas Recruiting
Goiânia, Goiás, Brazil
Contact: Sérgio Vencio    +55 62 3240-1900    sergio.vencio@icf.com.br   
Sponsors and Collaborators
Ache Laboratorios Farmaceuticos S.A.
Investigators
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Principal Investigator: Sérgio Alberto Cunha Vêncio Instituto de Ciências Farmacêuticas (ICF)

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Responsible Party: Ache Laboratorios Farmaceuticos S.A.
ClinicalTrials.gov Identifier: NCT03634514     History of Changes
Other Study ID Numbers: PPES 002/18
First Posted: August 16, 2018    Key Record Dates
Last Update Posted: August 17, 2018
Last Verified: August 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Additional relevant MeSH terms:
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Pain
Neurologic Manifestations
Signs and Symptoms
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs