Phase 1A Safety Trial of Inhaled PK10571 (GB002)

• Status: Completed
• Trial end date: 2018-12-03
• Target enrollment: 0
• Participant gender: All

Summary

This is a phase 1A randomized double blind placebo controlled single ascending dose and multiple ascending dose trial of inhaled PK10571 (GB002) in healthy adult subjects.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: GB002, Inc., a wholly owned subsidiary of Gossamer Bio, Inc.; Gossamer Bio Inc.
• Collaborators: Pulmokine Inc.; Worldwide Clinical Trials

Criteria

Inclusion Criteria:

• Males and females (if unable to become pregnant)

• Age 18-55

• Body mass index (BMI) 18-32 kg/m^2 and minimum weight of 50 kg (110 lbs)

• Non-smoker

• Ability to give informed consent

• Ability to remain in study unit for duration of study and return for outpatient visits

• Ability to use dry powder inhaler (DPI) effectively

(See full protocol for additional details.)

Exclusion Criteria:

• Hospitalization within the 6 months prior to the first dose of study treatment

• History or presence of clinically significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic, or psychiatric disease or any other condition that, in the opinion of the Investigator, would jeopardize the safety of the subject or the validity of the study results

• History or presence of active lung disease (i.e., asthma, chronic obstructive pulmonary disease [COPD], pulmonary fibrosis, hemoptysis, bronchiectasis) or prior intubation

• Currently uses an inhaler

• History or presence of heart disease (i.e., prior myocardial infarction [MI], coronary artery disease, heart failure, hypertension, pulmonary hypertension, valve disease, atrial fibrillation, other arrhythmia, or prolonged QT syndrome)

• History or presence of cancer (with the exception of basal cell skin cancer that has been effectively treated)

• History of diabetes mellitus

• History of thyroid disease other than hypothyroidism control with levothyroxine and documented normal thyroid-stimulating hormone (TSH)

• History of tuberculosis, Lyme disease, or other chronic or opportunistic infection.

• History of positive purified protein derivative (PPD) skin test, or positive PPD test at screening

• Has a positive test for hepatitis B surface antigen, hepatitis C antibody, or human immunodeficiency virus (HIV) at screening or has been previously treated for hepatitis B, hepatitis C, or HIV infection

• History of smoking within the past 15 years

• Is a female with a positive pregnancy test result, or who has the ability to become pregnant, or who is lactating

• Has forced expiratory volume in 1 second (FEV1) less than 80% predicted, forced vital capacity (FVC) ˂80% predicted, or resting oxygen saturation less than 97% on room air at screening or baseline

• Upper respiratory infection within the 3 months prior to the first dose of medication

• History of major bleeding or major surgical procedure of any type within 6 months prior to the first dose of medication

• History of minor bleeding disorders such as epistaxis, rectal bleeding (spots of blood on toilet paper), and gingival bleeding within 3 months before the study treatment

• History of bleeding disorder or coagulopathy

• Females with history of dysfunctional uterine bleeding, including history of menorrhagia or metrorrhagia, unless subject has had a hysterectomy.

• History of GI bleed

• Has used any over-the-counter (OTC) medication, nutritional or dietary supplements, herbal preparations, or vitamins within 7 days prior to the first dose of medication

• Has used any antiplatelet agents such as acetylsalicylic acid (ASA), nonsteroidal anti-inflammatory drugs (NSAIDs), clopidogrel (or similar agent) or anti-coagulants within 7 days prior to the first dose of medication

• Has used any prescription medication, except female hormonal replacement therapy, within 14 days prior to the first dose of study medication

• Has been treated with any known drugs that are moderate or strong inhibitors/inducers of CYP enzymes such as barbiturates, phenothiazines, cimetidine, carbamazepine, etc., within 30 days prior to the first dose of study medication and that in the Investigator's judgment may impact subject safety or the validity of the study results

• History of peripheral vascular disease

• History of autoimmune or collagen vascular disease

• History of sleep apnea

• History of clinically significant allergy to medications

• History of anaphylaxis

• History of liver disease

• History of alcohol or drug abuse

• Prolonged QTc on 12-lead ECG (i.e., QTc corrected using Fridericia's formula [QTcF] ˃450 msec), PR >210 msec, or QRS >110 msec at screening.

• Evidence of prior MI on ECG; presence of atrial fibrillation on ECG; presence of pre-excitation, 2nd or 3rd degree heart block, or abnormal waveform morphology that would preclude accurate measurement of the QT interval duration or other clinically significant abnormalities

• Chest x-ray reveals presence of infiltrate or other abnormality (mass, granuloma, fibrosis, pulmonary thickening, pleural effusion, pulmonary edema, wide mediastinum, cardiomegaly, or clinically significant increased interstitial markings)

• History of neurologic disorder (i.e., multiple sclerosis, amyotrophic lateral sclerosis [ALS], cerebrovascular accident [CVA], transient ischemic attach [TIA])

• History of deep vein thrombosis or pulmonary embolus

• History of clotting disorder

• History of mental illness requiring drug treatment or hospitalization

• History of renal failure or proteinuria (defined as 1+ proteinuria: ≥75 mg/dL on isolated urinalysis)

• Test results greater than the upper limit of normal (ULN) for AST, ALT, or total bilirubin

• Out of range results on the following coagulation tests: INR, prothrombin time (PT), or partial thromboplastin time (PTT)

• Total cholesterol >250 mg/dL or triglycerides >300 mg/dL at screening (based on fasting lipid profile)

• Estimated creatinine clearance less than 60 mL/min

• Hemoglobin at screening of <11.5 g/dl (if female subject) or <12.5 g/dl (if male subject)

• Has a clinically significant abnormal finding on the physical exam, medical history, electrocardiogram (ECG), or clinical laboratory results at screening. Note: Subjects with abnormal laboratory results not specifically excluded by this protocol may be enrolled if the Investigator deems the out-of-range values as not clinically significant

• History of treatment with a kinase inhibitor

• Has been on a significantly abnormal diet during the 4 weeks preceding the first dose of study medication

• Has donated blood or plasma within 30 days prior to the first dose of study medication

• Has participated in another clinical trial (randomized subjects only) within 30 days prior to the first dose of study medication

• Has a positive urine screen for drugs of abuse (amphetamines, barbiturates, benzodiazepines, cocaine, cannabinoids, opiates) or cotinine

• Vital signs (measured sitting after 3 minutes rest) at screening that are not within the following ranges (inclusive): heart rate: 40-100 beats per minute [bpm]; systolic blood pressure (BP): 90-145 mmHg; diastolic BP: 50-95 mmHg. Out-of-range vital signs may be repeated once. Blood pressure will be measured in both arms at screening, with a 3-minute rest between each measurement. Predose vital signs will be assessed by the Principal Investigator or designee (e.g., a medically qualified sub-investigator) prior to study drug administration. The Principal Investigator or designee will verify the eligibility of each subject with out-of-range vital signs and document approval prior to dosing

• Significant difference (i.e., greater than 15 mmHg) between the systolic blood pressure in each arm at screening

• History of lactose intolerance