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Randomized study of single and multiple doses of BBT002 in healthy volunteers and in adult patients with chronic obstructive pulmonary disease (COPD) or chronic rhinosinusitis with nasal polyps (CRSwNP).
This study a is a randomized, double-blinded, placebo-controlled single (SAD) and multiple-ascending dose (MAD) study to evaluate safety, tolerability, pharmacokinetics, immunogenicity, pharmacodynamics, and exploratory clinical activity of BBT002 in healthy volunteers (HVs) and in adult patients with COPD or CRSwNP. BBT002 is a drug candidate being developed for the treatment of COPD or CRSwNP. BBT002 will be given by intravenous injection or subcutaneous injection.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Part A: BBT002 | Experimental | A single dose of BBT002 will be administered in healthy volunteers |
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| Part B: BBT002 | Experimental | Multiple doses of BBT002 will be administered in healthy volunteers. |
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| Part C: BBT002 | Experimental | Multiple doses of BBT002 will be administered in patients with COPD |
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| Part A: Placebo | Placebo Comparator | A single dose of Placebo will be administered in healthy volunteers. |
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| Part B: Placebo | Placebo Comparator | Multiple doses of Placebo will be administered in healthy volunteers. |
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| Part C: Placebo | Placebo Comparator | Multiple doses of Placebo will be administered in patients with COPD. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BBT002 | Drug | BBT002 will be administered. |
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| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with adverse events following single and multiple administration of BBT002 | Incidence, relatedness, and severity of adverse events (AEs) graded per CTCAE v6.0. | Parts A and E - up to 141 days post first dose administration; Parts B, C, D, F, and G - up to 169 days post first dose administration |
| Number of participants with change in Laboratory assessments | Laboratory assessments include hematology, coagulation, clinical chemistry and urinalysis | Parts A and E - up to 141 days post first dose administration; Parts B, C, D, F, and G - up to 169 days post first dose administration |
| Number of participants with change in vital sign measurements following dose administration. | Blood pressure and heart rate will be assessed. | Parts A and E - up to 141 days post first dose administration; Parts B, C, D, F, and G - up to 169 days post first dose administration |
| Number of participants with change in physical examination following dose administration. | Physical examination will be assessed. | Parts A and E - up to 141 days post first dose administration; Parts B, C, D, F, and G - up to 169 days post first dose administration |
| Number of participants with change in 12-lead ECG readings | 12-lead ECG will be assessed. | Parts A and E - up to 141 days post first dose administration; Parts B, C, D, F, and G - up to 169 days post first dose administration |
| Measure | Description | Time Frame |
|---|---|---|
| PK parameters- maximum observed concentration (Cmax) | Maximum observed concentration of the study drug in serum will be analyzed for all subjects | At specified timepoints pre-dose and up to 169 days post first dose administration |
| PK parameters- Time of maximum observed Concentration (Tmax) |
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Key Inclusion Criteria (Parts A, B, C, D, E, F, and G)
Key Inclusion Criteria (Part C and F only) 1. Documented history of COPD with a post-bronchodilator Forced Expiratory Volume in 1 second/Forced Vital Capacity less than 0.70
Key Inclusion Criteria (Parts D and G)
1. Participants with confirmed diagnosis of CRSwNP
Key Exclusion Criteria for (Parts A, B, C, D, E, F, and G)
Key Exclusion Criteria (Part C and F only)
Key Exclusion Criteria (Parts D and G)
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Tracy Ji | Contact | +86 18001322760 | Tracy.Ji@bambusatx.com |
| Name | Affiliation | Role |
|---|---|---|
| Tracy Ji | Bambusa Therapeutics, Inc. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Equity Medical Bowling Green | Recruiting | Bowling Green | Kentucky | 42104 | United States |
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| Part D: Placebo | Placebo Comparator | Multiple doses of Placebo will be administered in patients with CRSwNP. |
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| Part E: Placebo | Placebo Comparator | Single dose of Placebo will be administered in healthy volunteers. |
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| Part F: Placebo | Placebo Comparator | Multiple doses of Placebo will be administered in patients with COPD. |
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| Part G: Placebo | Placebo Comparator | Multiple doses of Placebo will be administered in patients with CRSwNP. |
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| Part D: BBT002 | Experimental | Multiple doses of BBT002 will be administered in patients with CRSwNP. |
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| Part E: BBT002 | Experimental | Single dose of BBT002 will be administered in healthy volunteers. |
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| Part F: BBT002 | Experimental | Multiple doses of BBT002 will be administered in patients with COPD. |
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| Part G: BBT002 | Experimental | Multiple doses of BBT002 will be administered in patients with CRSwNP. |
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| Placebo | Drug | Placebo will be administered. |
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Serum PK Tmax will be analyzed for all subjects |
| At specified timepoints pre-dose and up to 169 days post first dose administration |
| PK parameters- Area under the curve (AUC) | Area under the curve of the study drug in serum will be analyzed for all subjects | At specified timepoints pre-dose and up to 169 days post first dose administration |
| PK parameters- Volume of distribution (Vz) | Volume of distribution of the study drug in serum will be analyzed for all subjects | At specified timepoints pre-dose and up to 169 days post first dose administration |
| PK parameters- Total clearance (CL) | Total clearance of the study drug in serum will be analyzed for all subjects | At specified timepoints pre-dose and up to 169 days post first dose administration |
| PK parameters- - Elimination Half-life (t1/2). | Elimination half-life of the study drug in serum will be analyzed for all subjects | At specified timepoints pre-dose and up to 169 days post first dose administration |
| The immunogenicity of BBT002 is measured as the number and percentage of subjects who develop Anti-Drug Antibodies (ADA). | Serum Anti-Drug Antibodies will be analyzed for all subjects | At specified timepoints pre-dose and up to 169 days post first dose administration |
| Equity Medical - Owensboro | Not yet recruiting | Owensboro | Kentucky | 42303 | United States |
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| Equity Medical LLC | Recruiting | New York | New York | 10023 | United States |
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| Linear Clinical Research | Recruiting | Perth | Western Australia | 6009 | Australia |
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| Momentum Clinical Research | Recruiting | Brisbane | 4068 | Australia |
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| Aleksandre Aladashvili Clinic LLC | Recruiting | Tbilisi | 0198 | Georgia |
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| Geo Hospitals Tbilisi Multiprofile Medical Center | Recruiting | Tbilisi | 0198 | Georgia |
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| LEPL The First University Clinic of Tbilisi State Medical University | Recruiting | Tbilisi | 0198 | Georgia |
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| Ltd Aversi Clinic | Recruiting | Tbilisi | 0198 | Georgia |
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| Momentum Clinical Research Hamilton | Not yet recruiting | Rotorua | Hamilton | 3010 | New Zealand |
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| Momentum Clinical Research | Recruiting | Pukekohe | 2120 | New Zealand |
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| Momentum Clinical Research | Recruiting | Wellington | 6021 | New Zealand |
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| Uniwersyteckie Centrum Kliniczne Osrodka Badan Klinicznych Wczesnych Faz | Not yet recruiting | Gdansk | 80-214 | Poland |
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| Centrum Nowoczesnych Terapii Dobry Lekarz Sp. z o.o. | Not yet recruiting | Krakow | 31-011 | Poland |
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| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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