Sofusa System With Sumatriptan (KC5010) Phase 1 Dose Escalation Safety and PK Study (KCC-SMT-002)

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

19 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-17

Study Completion Date

2018-03-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Study KCC-SMT-002, is a Phase 1, single-site, open-label, non-randomized, crossover, flexible dose design study to investigate the pharmacokinetic (PK) and safety comparing the Sofusa™ system with sumatriptan (KC5010) to Imitrex® oral tablets in 17 healthy volunteers.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

A Study to Evaluate the Pharmacokinetics and Bioequivalence of Sumatriptan Delivered Via the Intraject System

NCT00614029

Pharmacokinetics Bioequivalence

COMPLETED PHASE1

Safety & Efficacy of a Single Dose of Sumatriptan Powder Delivered Intranasally With the Bi-directional Device in Adults With Acute Migraine

NCT01462812

Migraine Headache

COMPLETED PHASE3

Efficacy and Safety of 20 mg Sumatriptan Powder Delivered Intranasally With the Bi-directional Device Compared With 100 mg Sumatriptan Tablets in Adults With Acute Migraine With or Without Aura

NCT01667679

Migraine Headaches

COMPLETED PHASE3

Sumatriptan Succinate 100 mg Tablets Under Fasting Conditions

NCT00847405

Healthy

COMPLETED PHASE1

Phase I Study to Compare NP101(Sumatriptan Iontophoretic Transdermal Patch) With Three Formulations of Imitrex®

NCT00546650

Healthy

COMPLETED PHASE1

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Migraine Disorders

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Sumatriptan Succinate Oral Tablet

100 mg oral tablet commercial Imitrex sumatriptan succinate tablet

Group Type ACTIVE_COMPARATOR

Sumatriptan Succinate Oral Tablet

Intervention Type DRUG

Sumatriptan succinate commercial Imitrex 100 mg tablet

Sofusa Profile #1

Combination device for transdermal delivery of sumatriptan succinate Current approved dose (SC)

Group Type EXPERIMENTAL

Transdermal delivery of sumatriptan succinate

Intervention Type COMBINATION_PRODUCT

Sumatriptan succinate transdermal drug delivery system

Sofusa Dose Profile #2

Combination device for transdermal delivery of sumatriptan succinate- adjust dose and flow rate to achieve PK profile based on results from Sofusa Dose Profile #1

Group Type EXPERIMENTAL

Transdermal delivery of sumatriptan succinate

Intervention Type COMBINATION_PRODUCT

Sumatriptan succinate transdermal drug delivery system

Sofusa Dose Profile #3

Combination device for transdermal delivery of sumatriptan succinate- adjust dose and flow rate to achieve PK profile based on results from Sofusa Dose Profile #2

Group Type EXPERIMENTAL

Transdermal delivery of sumatriptan succinate

Intervention Type COMBINATION_PRODUCT

Sumatriptan succinate transdermal drug delivery system

Sofusa Dose Profile #4

Combination device for transdermal delivery of sumatriptan succinate- adjust dose and flow rate to achieve PK profile based on results from Sofusa Dose Profile #3

Group Type EXPERIMENTAL

Transdermal delivery of sumatriptan succinate

Intervention Type COMBINATION_PRODUCT

Sumatriptan succinate transdermal drug delivery system

Sofusa Dose Profile #5

Combination device for transdermal delivery of sumatriptan succinate- adjust dose and flow rate to achieve PK profile based on results from prior Sofusa Dose Profile #2-4

Group Type EXPERIMENTAL

Transdermal delivery of sumatriptan succinate

Intervention Type COMBINATION_PRODUCT

Sumatriptan succinate transdermal drug delivery system

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Sumatriptan Succinate Oral Tablet

Sumatriptan succinate commercial Imitrex 100 mg tablet

Intervention Type DRUG

Transdermal delivery of sumatriptan succinate

Sumatriptan succinate transdermal drug delivery system

Intervention Type COMBINATION_PRODUCT

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Sofusa DoseDisc Sofusa DoseConnect KC5010

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Able to give voluntary written informed consent (personally signed and dated) and HIPPA Authorization prior to any study related procedures.
2. Available to participate for the entire study period.
3. Be a male or female person between 18 and 55 years (inclusive) of age.
4. Healthy as determined by the investigator based on a medical evaluation including history, physical examination, electrocardiogram (ECG), and laboratory tests.
5. Have systolic blood pressure (sitting) of \< 140 mmHg and diastolic blood pressure of \< 90 mmHg after 5 minutes of rest. Minor excursions in blood pressure outside of this range may be acceptable if determined not to be clinically significant by the study physician or medical monitor.
6. Have resting pulse rate (sitting) within normal range of 60-100 bpm. Minor excursions in resting pulse outside of this range may be acceptable if determined not to be clinically significant by the study physician or the medical monitor.
7. Females must be either postmenopausal for at least 1 year, surgically sterile (bilateral oophorectomy, tubal ligation, tubal occlusion, hysterectomy), or using adequate contraception from screening until 90 days after completion of study participation. Adequate contraception is defined as true abstinence, a vasectomized partner, or one of the following in combination with a diaphragm, cervical cap, or a condom:

* Hormonal contraceptives (oral, implant, patch, injection)
* Intrauterine device

Males must use adequate contraception and must not donate sperm from first admission to the clinical research center until 90 days after completion of study participation. Adequate contraception is defined as true abstinence, vasectomy, a partner who is surgically sterile (bilateral oophorectomy, tubal ligation, tubal occlusion, hysterectomy), or one of the following in combination with a diaphragm, cervical cap, or a condom:
* Hormonal contraceptives (oral, implant, patch, injection)
* Intrauterine device
8. Have a body weight above 50 kg and below 90 kg (inclusive).
9. Be able to communicate effectively with the study personnel and understand and comply with all study requirements.

Exclusion Criteria

1. Women who are pregnant or lactating.
2. Current use or has used tobacco- or nicotine-containing products (e.g., cigarettes, cigars, chewing tobacco, snuff, etc.) 30 days prior to investigational product administration. A cotinine test (with a cut-off of 200 mg) will be performed at screening and admission to the study center.
3. Recent history (i.e. within 2 years) of alcohol abuse, illicit drug use, or significant mental illness.
4. Positive screen for substances of abuse.
5. A positive screening result for human immunodeficiency virus (HIV) antibody, Hepatitis B surface antigen (HBsAg), or Hepatitis C antibody (anti-HCV).
6. Any disease or condition (medical or surgical) that might compromise a major body system (e.g. cardiovascular, respiratory, etc.) or conditions that may interfere with the absorption, distribution, metabolism, or excretion of the study medication.
7. Any bleeding disorders or use of anticoagulants.
8. Any conditions (e.g. diabetes, edema, scleroderma) or receiving medications (e.g. steroids, antibiotics) that alter skin integrity and/or healing. Any known condition or receiving medications causing hypo/hyperpigmentation or photosensitivity.
9. Presence or history of hypertension or other cardiovascular abnormalities such as, but not limited to, myocardial infarction, heart failure, arrhythmia, stroke, or peripheral vascular disease or any other cardiovascular disease that requires the subject to wear a pacemaker.
10. Use of a drug therapy known to induce or inhibit hepatic drug metabolism within 30 days prior to the Treatment visit for dosing.
11. Patient has received a live attenuated vaccine within the 4 weeks prior to treatment or plans to receive one during the study.
12. Febrile illness within 7 days of Treatment visit for dosing.
13. Has a positive history or known sensitivity to sumatriptan or other triptans.
14. Any history of sensitivity to methylene blue, fluorescein or calcein, or other similar dye product.
15. Subjects who have used ergotamine-containing or ergot-type medications (like dihydrogergotamine or methysergide) within the past week. The Imitrex® label specifies that these medication are contraindicated within 24 hours of use.
16. Diagnosed with ischemic bowel disease or severe hepatic impairment which are known contraindications to sumatriptan.
17. Concomitant therapy with the following medications which have significant drug interactions with sumatriptan: selective serotonin reuptake inhibitors (SSRIs), serotonin/norepinephrine reuptake inhibitor (SNRIs), tricyclic antidepressants, and monomine oxidase (MAO) inhibitors due to an increased risk of serotonin syndrome. Subjects receiving these medications may enroll in the study if these medications have been discontinued for 5 or more half-lives prior to the first Treatment visit.
18. Subjects who are currently taking prescription or over-the-counter medications (including vitamins and herbal preparations) that could interfere with the evaluation or the safety of the subject, as determined by the Investigator.
19. Participation in the treatment phase of a clinical study or receipt of an investigational drug or medical device within 30 days prior to the Treatment visit for dosing.
20. History of difficulty with phlebotomy procedures.
21. Donated blood (\>400 mL) or blood products within 45 days prior to the Treatment visit for dosing.
22. Subjects who have skin conditions or tattoos extensive enough to cover areas where the device is to be applied.
23. Any history of skin contact sensitivity to metals, plastics or adhesives.
24. Has a condition that, in the opinion of the Investigator, may increase the risk to the subject and/or the interpretation of the data.

Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes