Bioavailability of DHE Administered by I123 POD Device, IV Injection, and Migranal Nasal Spray in Healthy Adults

NCT ID: NCT03401346

Last Updated: 2019-03-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-10-19
• Study Completion Date: 2017-12-06

Brief Summary

A Phase I clinical trial to compare the bioavailability of dihydroergotamine mesylate (DHE) following a single dose administration of INP104 (DHE administered by I123 Precision Olfactory Delivery (POD) Device Nasal Spray) to that of D.H.E. 45 for Injection (Intravenous) and Migranal Nasal Spray in healthy adult subjects.

It is hypothesized that INP104 will address the current variability in nasal administration and give more reproducible dose delivery compared to Migranal nasal spray.

Blood concentrations of all three investigational products will be compared for 48 hours following dosing. The safety and tolerability of INP104 will be monitored throughout the study.

INP104 has been developed for the treatment of acute migraine headache. The device in which the drug will be delivered has been designed to deliver the medication to the upper nasal cavity with minimal variation in dose absorption, eg loss via dripping out of the nose or the dose being swallowed.

Approximately 36 participants in general good health (equal ratio of males and females desired) will be enrolled and will be allocated to receive 3 treatments in a randomized sequence. They will receive a single dose of INP104, a single dose of DHE via intravenous injection, and a single dose of Migranal Nasal Spray. There will be a wash out period where no treatment will be administered for 7 days in between each treatment. Participants are required to attend 3 inpatient periods and 1 final outpatient visit. Each participant will be in the study for up to 43 days.

Conditions

Migraine Headache

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

INP104

Single dose 1.45 mg Dihydroergotamine Mesylate (DHE), administered by I123 Precision Olfactory Delivery (POD) device nasal spray (INP104)

Group Type: EXPERIMENTAL

INP104

Intervention Type: COMBINATION_PRODUCT

Dihydroergotamine Mesylate (DHE) administered via I123 Precision Olfactory Delivery (POD) Device

D.H.E. 45 Injection (IV)

Single dose 1 mg Dihydroergotamine Mesylate (DHE) for intravenous injection

Group Type: ACTIVE_COMPARATOR

Dihydroergotamine Mesylate (DHE)

Intervention Type: DRUG

Dihydroergotamine Mesylate (DHE) injection (intravenous)

Migranal Nasal Spray

Single dose 2 mg Migranal Nasal Spray Dihydroergotamine Mesylate (DHE)

Group Type: ACTIVE_COMPARATOR

Migranal Nasal Spray

Intervention Type: COMBINATION_PRODUCT

Dihydroergotamine Mesylate (DHE) delivered via Migranal Nasal Spray pump

Interventions

INP104

Dihydroergotamine Mesylate (DHE) administered via I123 Precision Olfactory Delivery (POD) Device

Intervention Type: COMBINATION_PRODUCT

Dihydroergotamine Mesylate (DHE)

Dihydroergotamine Mesylate (DHE) injection (intravenous)

Intervention Type: DRUG

Migranal Nasal Spray

Dihydroergotamine Mesylate (DHE) delivered via Migranal Nasal Spray pump

Intervention Type: COMBINATION_PRODUCT

Eligibility Criteria

Inclusion Criteria

• Adult male and females, 18 to 55 years of age (inclusive) at the time of screening.
• Subjects must be in good general health, with no significant medical history (including migraine), have no clinically significant abnormalities on physical examination at screening, and/or before administration of the initial dose of investigational product.
• Subjects must have a Body Mass Index (BMI) between 18 and 32 kg/m2, inclusive.
• Subjects must have clinical laboratory values within normal range as specified by the testing laboratory, or assessed as not clinically significant by the Principal Investigator.
• Negative urine drug screen/alcohol breath test at screening.
• Subjects who are willing to refrain from smoking for the duration of the study.

Exclusion Criteria

• Subjects with a recent history of migraine and its variants including hemiplegic migraine and basilar migraine. A recent history of migraine is defined as (a) current or past history of migraine with at least 1 attack in last 6 months or (b) those receiving antimigraine prophylaxis.
• Positive testing for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C antibodies (HCV).
• Subjects who have ingested caffeine within 48 hours before admission on Day -1. Subjects must also agree to refrain from consumption of caffeinated drinks for 48 hours before admission of Days 7 and 14 (i.e. prior to each subsequent dosing), and throughout confinement.
• Subjects with ischemic heart disease or subjects who have clinical symptoms or findings consistent with coronary artery vasospasm including Prinzmetal's variant angina.
• Subjects with hypertension, known peripheral arterial disease, Raynaud's phenomenon, sepsis, history of vascular surgery or severely impaired hepatic or renal function
• Subjects who have previously shown hypersensitivity to ergot alkaloids or metoclopramide.
• Use of any relevant prescription, over-the-counter medication (with the exception of oral contraceptives), foods (e.g. grapefruit juice) or supplements (including herbal) within 14 days of randomization [especially those affecting the Cytochrome P450 3A4 (CYP3A4) metabolic pathway].
• History or presence of alcoholism or drug abuse within the 2 years prior to the first investigational product administration.
• Surgery within the past three months prior to the first investigational product administration as determined by the PI to be clinically relevant.
• Active infection and/or use of macrolide antibiotics within 14 days prior to enrollment.
• History of recurrent infections.
• Any nasal congestion or physical blockage in either nostril, or deviated nasal septum as determined by nasal examination.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Impel Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jason Lickliter, MD

Role: PRINCIPAL_INVESTIGATOR

Centre for Clinical Studies/Nucleus Network

Locations

Centre for Clinical Studies/Nucleus Network

Melbourne, Victoria, Australia

Countries

Australia

References

Shrewsbury SB, Jeleva M, Satterly KH, Lickliter J, Hoekman J. STOP 101: A Phase 1, Randomized, Open-Label, Comparative Bioavailability Study of INP104, Dihydroergotamine Mesylate (DHE) Administered Intranasally by a I123 Precision Olfactory Delivery (POD(R) ) Device, in Healthy Adult Subjects. Headache. 2019 Mar;59(3):394-409. doi: 10.1111/head.13476. Epub 2019 Jan 19.

Reference Type: DERIVED

PMID: 30659611 (View on PubMed)

Other Identifiers

ACTRN12617001381370p

Identifier Type: REGISTRY

Identifier Source: secondary_id

INP104-101

Identifier Type: -

Identifier Source: org_study_id