A Study to Assess the Safety, Tolerability, and Pharmacokinetics of PUR3100 in Health Adults

NCT05351086 | Completed Phase 1 FDA Drug

• 1 other identifier: 601-0022
• Study Type: interventional
• Target: 26
• Locations: 1 country
• Sites: 1

Brief Summary

A Double Dummy, Double-blind Study to Assess the Safety, Tolerability, and Pharmacokinetics of PUR3100 in Healthy Adults

Conditions

Healthy

Outcome Measures

Primary Outcomes (9)

• Safety and Tolerability

  To determine the safety and tolerability of single doses of inhaled PUR3100 in healthy through the review of AEs

  Day 1 through Day 3adult subjects

• Maximum Plasma Concentration [Cmax]

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects by measuring the maximum drug concentration in blood plasma. This will also be compared to Cmax of participants who receive IV D.H.E. 45.

  Day 1 through Day 3

• Last Observed Plasma Concentration [Clast]

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects by measuring the last observed quantifiable concentration of PUR 3100 in blood plasma. This will also be compared to Clast of participants who receive IV D.H.E. 45.

  Day 1 through Day 3

• Time to Peak Drug Concentration [Tmax]

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects by measuring the time time it takes for a drug to reach the maximum concentration (Cmax). This will also be compared to Tmax of participants who receive IV D.H.E. 45.

  Day 1 through Day 3

• Time of last measurable concentration [Tlast]

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects by measuring the time time it takes for a drug to reach the last measurable concentration of PUR 3100 in blood plasma. This will also be compared to Tlast of participants who receive IV D.H.E. 45.

  Day 1 through Day 3

• Area under the curve [AUC (0-t), AUC (0-inf), AUC (0-2h)]

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects by measuring the drug concentration in blood plasma over time. This will also be compared to the AUC (0-t), AUC (0-inf), and AUC (0-2h) of participants who receive IV D.H.E. 45.

  Day 1 through Day 3

• Half Life [ t 1/2 ]

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects by measuring the time it takes for the amount of drug in the blood to reduce by 50%. This will also be compared to the half life of participants who receive IV D.H.E. 45.

  Day 1 through 3

• Clearance (CL/F)

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects. This will also be compared to the CL/F of participants who receive IV D.H.E. 45.

  Day 1 through Day 3

• Apparent Volume of Distribution During Terminal Phase (Vz/F)

  To characterize the systemic pharmacokinetics (PK) of single doses of inhaled PUR3100 in healthy adult subjects. This will also be compared to the Vz/F of participants who receive IV D.H.E. 45.

  Day 1 through Day 3

Study Arms (4)

Inhaled placebo and IV D.H.E. 45 1 mg

EXPERIMENTAL

Drug: Dihydroergotamine (D.H.E 45); Other: Matching Placebo for PUR3100

Inhaled PUR3100 0.5 mg and IV placebo

EXPERIMENTAL

Drug: PUR3100; Other: Matching Placebo for D.H.E 45

Inhaled PUR3100 1.0 mg and IV placebo

EXPERIMENTAL

Drug: PUR3100; Other: Matching Placebo for D.H.E 45

Inhaled PUR3100 1.5 mg and IV placebo

EXPERIMENTAL

Drug: PUR3100; Other: Matching Placebo for D.H.E 45

Interventions

PUR3100 DRUG

PUR3100 is an inhalation powder containing DHE, an anti-migraine treatment with broad spectrum agonist activity against 5-hydroxytryptamine (5-HT), dopamine, and adrenergic receptors. PUR3100 is provided as 500 µg dose strength capsules. Each capsule contains the drug substance, DHE mesylate, with mannitol, leucine, and sodium chloride as excipients.

Inhaled PUR3100 0.5 mg and IV placebo; Inhaled PUR3100 1.0 mg and IV placebo; Inhaled PUR3100 1.5 mg and IV placebo

Dihydroergotamine (D.H.E 45) DRUG

D.H.E. 45 is ergotamine hydrogenated in the 9, 10 position as the mesylate salt. It is supplied as a clear, colorless solution supplied in sterile ampules for IV, intramuscular, or subcutaneous administration containing (per mL) DHE mesylate, USP 1 mg, ethanol, 94% w/w. 6.2% by volume, glycerin 15% by weight, and water for injection.

Inhaled placebo and IV D.H.E. 45 1 mg

Matching Placebo for PUR3100 OTHER

Each capsule of matching placebo is filled with iSPERSE powder comprised of mannitol, leucine, and sodium chloride. The PUR3100 inhalation powder is administered using the supplied RS01 inhalation device (RS01 UHR2, Plastiape S.p.A.).

Inhaled placebo and IV D.H.E. 45 1 mg

Matching Placebo for D.H.E 45 OTHER

The matching placebo for D.H.E. 45 is 0.9% sterile saline for injection.

Inhaled PUR3100 0.5 mg and IV placebo; Inhaled PUR3100 1.0 mg and IV placebo; Inhaled PUR3100 1.5 mg and IV placebo

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male or female subjects aged 18 to 55 years of age with a body mass index ≥17 and ≤35 kg/m2.
• Subject has normal screening and baseline blood pressure, defined as a systolic value ≥90 mmHg and ≤140 mmHg and a diastolic value \>60 mmHg and \<90 mmHg.
• Female subjects who are of childbearing potential and male subjects with female partner(s) of childbearing potential must agree to use an effective contraceptive throughout the study (e.g., oral contraceptives or Norplant®; a reliable double barrier method of birth control \[diaphragms with contraceptive jelly; cervical caps with contraceptive jelly; condoms with contraceptive foam\]; intrauterine devices; partner with vasectomy; or abstinence) and for at least 90 days after study drug administration. In addition, female subjects must have a negative serum pregnancy test at screening and a negative urine pregnancy test prior to dosing. Note: Women of non-childbearing potential may be enrolled if they are:
• Surgically sterile (e.g., hysterectomy with or without oophorectomy; fallopian tube ligation; endometrial ablation), for at least 30 days prior to signing the ICF
• Post-menopausal (≥ 12 consecutive months of spontaneous amenorrhea and \> 50 years of age)
• Female subjects must agree not to donate ova/oocytes during the study and for 90 days after the last dose of IMP.
• Male subject must agree not to donate semen during the study and for 90 days after the last dose of IMP.
• Subject is able and willing to abstain from alcohol for 48 hours prior to admission to the study unit and throughout the entire study until completion of the Day 7 follow up visit.
• Subject is willing to participate in the study, comply with the study requirements, and voluntarily provide written informed consent.
• Subject can read, write, and speak English.
• Subject is mentally competent to provide informed consent.
• Subject can perform technically acceptable spirometry at screening.
• Subject can demonstrate the correct inhalation technique for use of the delivery device and to generate sufficient peak inspiratory flow (PIF) of at least 40 L/min using the In-Check DIAL device at screening.

You may not qualify if:

• Subject has a history of proven or suspected coronary artery disease (CAD), coronary vasospasm (including Prinzmetal's angina), peripheral vascular disease, or other ischemic diseases (e.g., ischemic bowel syndrome or Raynaud's syndrome) or cardiac disorder (e.g., any clinically significant dysrhythmia), any history of heart attack or stroke, hypertension, diabetes mellitus, liver or kidney disease, aortic aneurysm, chronic pulmonary disease, or recent (within 3 months) sepsis or vascular surgery.
• Subject has a current diagnosis of asthma, chronic obstructive pulmonary disease, active tuberculosis, lung cancer, bronchiectasis, sarcoidosis, lung fibrosis, interstitial lung disease, known alpha-1 antitrypsin deficiency, or other active pulmonary disease.
• Subject has clinically significant abnormal laboratory values at screening that, in the opinion of the investigator would make the subject inappropriate for the study or put the subject at undue risk, specifically liver function tests (LFTs) \>1.5 times the upper limit of normal (ULN); hemoglobin \<10 gm/dL; absolute neutrophil count (ANC) \<2.0 x 109/L; white blood cells (WBC) ˃11 x 109/L; platelets \<100,000 or \>500,000; international normalization ratio (INR) \>1.3.
• Subject has a QTcF of \>450 msec in males or \>470 msec in females at screening.
• Subject has forced expiratory volume in 1 second (FEV1) or forced vital capacity (FVC) on screening spirometry that is less than 80% predicted.
• Subject has a history of illicit drug or alcohol abuse within the past 12 months prior to screening.
• Subject smokes more than 5 cigarettes per day or vapes more than 5 times per day with devices that deliver nicotine.
• Subject has a history of nicotine replacement products daily within 6 months prior to screening.
• Subject has a positive alcohol test result at screening.
• Subject has a positive urine drug test result at screening, unless the result can be explained by the subject's current medications, in which case the PI should discuss the disposition of the subject with the Sponsor. Cannabidiol (CDB) and tetrahydro cannabinol (THC) use is prohibited.
• Subject has a known sensitivity to the study drug or any of the excipients of the formulation, or history of clinically significant sensitivity to any agent that, in the opinion of the investigator, would make participation in the study inadvisable.
• Subject has donated blood or blood products or had substantial loss of blood (more than 500 mL) within 6 weeks prior to screening.
• Subject has participated in an interventional study involving an experimental therapeutic agent within 3 months of screening.
• Women who have a positive serum β-human chorionic gonadotropin (hCG) pregnancy test at screening or a positive urinary hCG pregnancy test prior to dosing, is pregnant, lactating, or planning to become pregnant during the study or within 90 days after conclusion of study participation.
• Subject has a positive hepatitis B surface antigen (HbsAg), hepatitis C virus (HCV) antibody or human immunodeficiency virus (HIV) test result. Subjects who are hepatitis B surface (HBs) antibody positive or hepatitis B (HB) core antibody positive are not excluded provided the HBsAg result is negative. Subjects who are HCV antibody positive are not excluded if a subsequent HCV RNA test is negative.

Sponsors & Collaborators

• Pulmatrix Inc.: lead

Study Sites (1)

Nucleus Network Melbourne

Melbourne, Victoria, 3004, Australia

Location

MeSH Terms

Interventions

Dihydroergotamine

Intervention Hierarchy (Ancestors)

Ergotamines; Ergot Alkaloids; Alkaloids; Heterocyclic Compounds; Heterocyclic Compounds, 4 or More Rings; Heterocyclic Compounds, Fused-Ring

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Masking Details: A computerized randomization scheme will be created and shall be considered blinded (as per the following). The randomization is available only to the clinical research unit pharmacy staff that are preparing the drug who will not be involved in any other aspect of the study including administration of the drug. It will not be made available to the subjects, site PI, or members of the staff responsible for the monitoring and evaluation of study assessments.
• Purpose: TREATMENT
• Intervention Model: FACTORIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Double Dummy, Double-blind

Study Record Dates

• First Submitted: April 19, 2022
• First Posted: April 28, 2022
• Study Start: June 9, 2022
• Primary Completion: September 22, 2022
• Study Completion: September 22, 2022
• Last Updated: December 23, 2022

Record last verified: 2022-12

Data Sharing

• IPD Sharing: Will not share

Locations

AU (1)