Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of BOS161721 in Healthy Subjects

NCT ID: NCT03036865

Last Updated: 2020-11-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 61 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-01-31
• Study Completion Date: 2018-04-27

Brief Summary

Study BOS161721-01 is a randomized, single center, double-blind, placebo-controlled trial conducted to study the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of single ascending intravenous (IV) and subcutaneous (SC) doses of BOS161721 or placebo in healthy adult male and female participants.

Detailed Description

Study BOS161721-01 will consist of 7 single ascending dose (SAD) cohorts, each with 8 participants (6 active:2 placebo), and an eighth SAD cohort with 5 participants (all active). Participants will be randomized in a 3:1 ratio (BOS161721:placebo) and will either receive a single dose of BOS161721 (1, 3, 10, 22, 30, 60, 120, or 240 milligrams [mg]) or placebo. Participants in Cohort 1 will receive the lowest dose, administered IV (1 mg), followed by Cohort 2, in which participants will receive the second lowest dose, administered SC (3 mg). BOS161721 or placebo will also be administered SC in Cohorts 3, 4, 5, 7, and 8. Participants in Cohort 6 will be administered an IV dose of 22 mg (5 active) in parallel to the 60 mg SC-dosed fifth cohort. This dose has been selected to generate a similar exposure to that following the 30 mg SC dose. The actual Cohort 6 IV dose may be adjusted upon available PK data.

Participants will be in this study for up to 56 weeks, which includes a Screening Period of up to 28 days, a single-dose treatment day (during the in-subject treatment period), and a 52-week post-treatment Follow-up Period, which is required due to the potential half-life of BOS161721.

Conditions

Healthy Participants

Keywords

Healthy participants; BOS161721; Pharmacokinetics; Pharmacodynamics

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: TRIPLE

Study Groups

Cohort 1: 1 mg, IV BOS161721

Each participant will receive a single intravenous (IV) dose of BOS161721 1 milligram (mg).

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 1: matching placebo

Each participant will receive matching IV placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 2: 3 mg, SC BOS161721

Each participant will receive a single subcutaneous (SC) dose of BOS161721 3 mg.

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 2: matching placebo

Each participant will receive matching SC placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 3: 10 mg, SC BOS161721

Each participant will receive a single SC dose of BOS161721 10 mg.

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 3: matching placebo

Each participant will receive matching SC placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 4: 30 mg, SC BOS161721

Each participant will receive a single SC dose of BOS161721 30 mg.

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 4: matching placebo

Each participant will receive matching SC placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 5: 60 mg, SC BOS161721

Each participant will receive a single SC dose of BOS161721 60 mg.

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 5: matching placebo

Each participant will receive matching SC placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 6: 22 mg, IV BOS161721

Each participant will receive a single IV dose of BOS161721 22 mg.

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 7: 120 mg, SC BOS161721

Each participant will receive a single SC dose of BOS161721 120 mg.

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 7: matching placebo

Each participant will receive matching SC placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 8: 240 mg, SC BOS161721

Each participant will receive a single SC dose of BOS161721 240 mg.

Group Type: EXPERIMENTAL

BOS161721

Intervention Type: DRUG

Single dose administered IV or SC

Cohort 8: matching placebo

Each participant will receive matching SC placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Single dose administered IV or SC

Interventions

BOS161721

Single dose administered IV or SC

Intervention Type: DRUG

Placebo

Single dose administered IV or SC

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Participant voluntarily agrees to participate in this study and signs an Institutional Review Board (IRB)-approved informed consent prior to performing any of the Screening procedures
• Participants should be between 18 and 55 years (both inclusive) of age at the time of Screening, with a body mass index (BMI) between 17.5 and 32 kilograms per meters squared (kg/m^2) (both inclusive) at the time of Screening, have a weight > 50 kg and < 120 kg at the time of Screening, and be in general good health at least 8 weeks prior to the Screening visit. Good health is defined as individuals without known disease(s) as determined by a responsible physician, based on medical evaluation, including medical history, physical examination, laboratory tests, imaging, and cardiac monitoring.
• Women of non-childbearing potential status:

• Hysterectomy;
• Bilateral tubal ligation/tubal occlusion;
• Bilateral salpingectomy;
• Bilateral oophorectomy;
• Postmenopausal - defined as 12 months of spontaneous amenorrhea (In questionable cases, a blood sample will be taken with simultaneous testing of follicle-stimulating hormone (FSH) and estradiol levels, which should be consistent with menopausal range.)
• Women of childbearing potential will be allowed to participate and have to agree to use at least 1 of the following contraception methods at all times throughout study participation in addition to either a condom with spermicide or a diaphragm/cervical cap with spermicide:

• Non-hormonal intrauterine device (IUD; Paragard®/copper)
• Hormonal IUD (Mirena®)
• Nexplanon® or implantation - progesterone inserts under the skin
• Males will either be sterile, agree to be abstinent from Day -1 through the last study visit, or agree to use 2 highly effective methods of contraception such as:

• A male condom with spermicide;
• A sterile sexual partner;
• Use by female sexual partner of an IUD with spermicide; a female condom with spermicide; contraceptive sponge with spermicide; an intravaginal system; a diaphragm with spermicide; a cervical cap with spermicide; or oral, implantable, transdermal, or injectable contraceptive(s).
• Non-smokers or people who smoke up to 5 cigarettes per day but less than 10 packs per year
• Participants should be willing and able to comply with all study procedures. The criterion for inclusion will be reviewed and verified at Screening and admission.

Exclusion Criteria

• Prior clinical trial experience with monoclonal antibodies if there were clinically relevant tolerability issues with previous administration or if a washout period of 60 days or 5 half-lives (whichever is longer) has not occurred prior to the planned first day of dosing
• History of any autoimmune disease (e.g., rheumatoid arthritis, Lupus)
• History or current diagnosis of cancer, with the exception of non-melanoma skin cancer or cervical cancer in situ treated with apparent success with curative therapy (response duration > 5 years)
• Asthma, currently treated with or in the opinion of the Principal Investigator likely to require additional systemic glucocorticosteroid therapy during the study, is exclusionary.
• History of any clinically important drug or vaccine allergy or anaphylaxis
• A cluster of differentiation 4 (CD4+) lymphocyte count < 500 cell/millimeters cubed (mm^3) at Screening
• Positive anti-keyhole limpet hemocyanin (KLH) antibodies at Screening
• Previous immunization with KLH
• Known allergy to shellfish, KLH vaccine, or hypersensitivity to proteins foreign to the body
• Levels of Immunoglobulin G (IgG) and Immunoglobulin M (IgM) outside of reference value deemed clinically significant by the Principal Investigator at Screening
• History or sensitivity to heparin or heparin-induced thrombocytopenia
• Participants with cryptosporidium in the stool sample at Screening
• Abnormal bilirubin or alanine aminotransferase (ALT) at Screening as judged by the Principal Investigator to be clinically significant
• Positive urine drug screen at Screening or Day -1
• History of alcohol dependence as determined by a positive alcohol serum test at Screening or Day -1 or participants who consume more than 14 (female participants) or 21 (male participants) units of alcohol a week (unit = 1 glass of wine [125 milliliters (mL)/4 ounces] = 1 measure [25 mL/1 ounce] of spirits = 284 mL [10 ounces] of beer)
• Participants who have a positive test, or have been treated, for Hepatitis A, Hepatitis B, Hepatitis C virus, human immunodeficiency virus (HIV), cytomegalovirus (CMV) or Epstein-Barr virus (EBV). Regarding Hepatitis B, any of the following would exclude the participant from the study:

• Participants with positive Hepatitis B Surface antigen (HBsAg);
• Participants with Hepatitis B DNA levels > 200 copies/mL (quantified by real-time polymerase chain reaction) in case the participant is positive for Hepatitis B surface antibody (HBsAb) but negative for HBsAg;
• Positive for Hepatitis B core antibody (HBcAb)
• Current clinical, radiographic, or laboratory evidence of active tuberculosis (TB)
• A history of active TB within the last 3 years before Screening, even if treated
• Therapy for latent TB that has not been completed as per local country guidelines
• Positive interferon gamma release assay (IGRA) for TB unless proper treatment is documented, as described above
• Donation of blood (> 500 mL) or blood products within 2 months (56 days) prior to Day -1
• Any medically relevant pre-existing condition that could jeopardize the safety of the participant during the trial
• Any participant, on the judgment of the Principal Investigator, who would be considered unsuitable for the clinical trial
• A shingles infection in the last 6 months prior to Screening
• Live vaccination or use of steroids in the last 2 months prior to Screening
• Use of prescription medications (except for oral contraceptive) and over-the-counter treatments, including herbal supplements such as St. John's Wart (except multivitamins), in the 2 weeks prior to Screening
• Participants with poor dental health and/or severe foot fungal infections, as judged by the Principal Investigator

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

Sponsors

Boston Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Baltimore, Maryland, United States

Countries

United States

References

Hussaini A, Mukherjee R, Berdieva DM, Glogowski C, Mountfield R, Ho PTC. A Double-Blind, Phase I, Single Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of BOS161721 in Healthy Subjects. Clin Transl Sci. 2020 Mar;13(2):337-344. doi: 10.1111/cts.12715. Epub 2019 Nov 29.

Reference Type: DERIVED

PMID: 31664766 (View on PubMed)

Other Identifiers

PXL232187

Identifier Type: OTHER

Identifier Source: secondary_id

BOS161721-01

Identifier Type: -

Identifier Source: org_study_id