Working...
ClinicalTrials.gov
ClinicalTrials.gov Menu

Study to Evaluate EB-001 in Reducing Musculoskeletal Pain

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT03193593
Recruitment Status : Completed
First Posted : June 21, 2017
Results First Posted : January 25, 2019
Last Update Posted : January 25, 2019
Sponsor:
Information provided by (Responsible Party):
Bonti, Inc.

Brief Summary:
To determine the safety and efficacy of single intra-operative treatment of EB-001 IM injections into the Pectoralis Major (PM) in subjects undergoing breast augmentation with subpectoral implants

Condition or disease Intervention/treatment Phase
Musculoskeletal Pain Drug: Placebo Drug: EB-001 Phase 2

Detailed Description:

This study will evaluate the safety and efficacy of EB-001 in decreasing post-surgical pain in patients undergoing surgical breast augmentation with subpectoral placement of the implants. Intramuscular (IM) injection of EB-001 into the PM bilaterally during surgery may decrease pain related to stretching of the PM by the implants.

The safety objective is to determine the safety and tolerability of single intraoperative treatment of EB-001 IM injections into the PM in subjects undergoing breast augmentation with subpectoral implants.

The efficacy objective is to evaluate the efficacy of intraoperative administration of EB-001 IM into the PM in reducing the pain and use of rescue pain medications in subjects undergoing breast augmentation with subpectoral implants.


Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 66 participants
Allocation: Randomized
Intervention Model: Sequential Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Phase 2 Placebo-Controlled, Double Blind, Ascending Dose Cohort Study to Evaluate Safety and Efficacy of EB-001 IM Injections in Reducing Musculoskeletal Pain in Subjects Undergoing Elective Augmentation Mammoplasty (Breast Augmentation)
Actual Study Start Date : August 29, 2017
Actual Primary Completion Date : April 26, 2018
Actual Study Completion Date : August 7, 2018

Arm Intervention/treatment
Placebo Comparator: Placebo Injections

Intervention: Drug: Placebo

Single Saline Injection into the Pectoralis Muscle

Drug: Placebo
Placebo- Single injection of saline into Pectoralis Muscle

Active Comparator: EB-001 Dose 1

Intervention: Drug: EB-001

1st Dose in escalation paradigm. Single Injection of active drug into the pectoralis muscle

Drug: EB-001
Single injection of EB-001 into Pectoralis Muscle

Active Comparator: EB-001 Dose 2 (1.6X)

Intervention: Drug: EB-001

2nd Dose in escalation paradigm, 1.6X Dose 1. Single Injection of active drug into the pectoralis muscle

Drug: EB-001
Single injection of EB-001 into Pectoralis Muscle

Active Comparator: EB-001 Dose 3 (3.3X)

Intervention: Drug: EB-001

3rd Dose in escalation paradigm, 3.3X Dose 1. Single Injection of active drug into the pectoralis muscle

Drug: EB-001
Single injection of EB-001 into Pectoralis Muscle

Active Comparator: EB-001 Dose 4 (6.7X)

Intervention: Drug: EB-001

4th Dose in escalation paradigm, 6.7X Dose 1. Single Injection of active drug into the pectoralis muscle

Drug: EB-001
Single injection of EB-001 into Pectoralis Muscle

Active Comparator: EB-001 Dose 5 (10X)

Intervention: Drug: EB-001

5th Dose in escalation paradigm, 10X Dose 1. Single Injection of active drug into the pectoralis muscle

Drug: EB-001
Single injection of EB-001 into Pectoralis Muscle

Active Comparator: EB-001 Dose 6 (13.3X)

Intervention: Drug: EB-001

6th Dose in escalation paradigm, 13.3X Dose 1. Single Injection of active drug into the pectoralis muscle

Drug: EB-001
Single injection of EB-001 into Pectoralis Muscle




Primary Outcome Measures :
  1. Subject's Assessment of Pain Using the Numeric Pain Rating Scale (AUC16h-96h) [ Time Frame: 16 hours to 96 hours following dosing ]
    Subject's assessment of pain using the Numeric Pain Rating Scale (1= No Pain, 10= Maximum Pain) for the first 96 hours following injection, expressed as AUC over the 16h to 96h period following dosing.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Women 18 to 55 years of age, inclusive
  2. Women who are in good health as determined by medical history, physical examination, clinical laboratory studies, ECGs, vital signs, and Investigator judgment
  3. Scheduled to undergo primary breast augmentation under general anesthesia (endotracheal or otherwise) with:

    1. Sub-pectoral implants placement,
    2. Infra-mammary surgical approach,
    3. Implant size between 250 and 400cc and
    4. Non-textured saline breast implants
  4. American Society of Anesthesiologist (ASA) Physical Class 1-2
  5. Women of non-childbearing potential or postmenopausal (at least 12 consecutive months of amenorrhea)
  6. Women of childbearing potential must not be pregnant, lactating, or planning to become pregnant during the study
  7. Women of childbearing potential agreeing to use either:

    1. a highly effective method of contraception with failures rates less than 1% per year such as implant, intrauterine device (IUD), or confirmed sterilization and sterilization procedure at least 3 months prior to the day of dosing
    2. dual methods of contraception with overall failures rate less than 1% per year such as injectable, pill, patch, ring, and diaphragm from the day of dosing for 3 months (subjects using oral contraception must have initiated treatment at least 2 months prior to the day of dosing)
  8. Willing and able to complete protocol requirements and instructions, which includes completion of all required visits, procedures and in-clinic stays until the end of the study
  9. Willing and able to sign and date IRB-approved informed consent
  10. Able to speak, read, and understand the language of the informed consent form (ICF) and study questionnaires

Exclusion Criteria:

  1. History of surgical procedure involving the breast, including, but not limited to, breast augmentation. History of minor localized breast biopsy is not exclusionary if it occurred at least 1 year prior to the screening visit, and if considered not clinically significant in the opinion of the investigator.
  2. Pre-existing lung disease that could impact subject safety in the opinion of the investigator
  3. History of smoking within the past two years
  4. Slow vital capacity that is below 80% of normal value for respective race, age, height, and gender
  5. Pulse oximetry below 95%
  6. Body weight less than 50 kg (110 pounds) or a Body Mass Index (BMI) of ≥ 32
  7. Documented diagnosis of chronic pain condition, or other painful pre-operative condition that, in the opinion of the investigator, may require analgesic treatment in the post-operative period (e.g. significant joint pain, neuropathic pain)
  8. Known hypersensitivity to any botulinum toxin serotype or to any component of the formulation
  9. Reported use of any botulinum toxin within 3 months prior to the date of surgery
  10. Anticipated use of any botulinum toxin of any serotype during the study
  11. Use of long acting opioids within 3 days or any opioid medication within 24 hours prior to surgery
  12. Aminoglycoside intake within 48 hours prior to or during surgery
  13. Pre-existing disorders of the neuromuscular junction (myasthenia gravis, Eaton- Lambert syndrome, or amyotrophic lateral Sclerosis)
  14. Any past or current medical condition that in opinion of investigator, puts subject at undue safety risk for surgical complications or for use of the investigational product.
  15. Any clinically significant psychiatric condition that, in opinion of investigator, may interfere with study assessments or protocol compliance
  16. History of alcohol or drug abuse in the last 3 years, based on investigator judgement
  17. Current enrollment in an investigational drug or device study or participation in such a study within 30 days or 5 half-lives of the drug, whichever is longer, of entry into this study
  18. Subject plans to donate blood or plasma from 30 days prior to screening until last follow-up visit (Day 29)
  19. Reported pain score of 2 or more at screening on the 11-point scale NPRS-A following strength testing with PM activation

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): NCT03193593


Locations
Layout table for location information
United States, California
Lotus Clinical Research
Pasadena, California, United States, 91105
Sponsors and Collaborators
Bonti, Inc.
  Study Documents (Full-Text)

Documents provided by Bonti, Inc.:

Layout table for additonal information
Responsible Party: Bonti, Inc.
ClinicalTrials.gov Identifier: NCT03193593     History of Changes
Other Study ID Numbers: EB001-MA201
First Posted: June 21, 2017    Key Record Dates
Results First Posted: January 25, 2019
Last Update Posted: January 25, 2019
Last Verified: January 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Layout table for MeSH terms
Musculoskeletal Pain
Muscular Diseases
Musculoskeletal Diseases
Pain
Neurologic Manifestations
Signs and Symptoms