Phase 1
N=112
A SAD/MAD Study of Safety, Tolerability and Pharmacologic Activity of BT200 in Normal Volunteers
Cerebrovascular Stroke · Large-Artery Atherosclerosis (Embolus/Thrombosis) · Intracranial Arteriosclerosis
Bottom Line
View on ClinicalTrials.gov: NCT04103034 ↗Enrolled (actual)
112
Serious AEs
3.6%
Results posted
Mar 2024
Primary outcome: Primary: Number of Participants With Treatment-related Adverse Events as Assessed by CTCAE v4.0 — 0; 1; 0; 1 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 1
- Interventions
- BT200 (Drug); Desmopressin (Drug); Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Band Therapeutics
- Primary completion
- Sep 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Treatment-related Adverse Events as Assessed by CTCAE v4.0 |
0; 1; 0; 1; 1; 0 | — |
| SECONDARY Measured Area Under the Curve (AUC) |
1.159; 5.405; 11.50; 64.39; 161.6; 259.5 | — |
| SECONDARY Maximum Plasma Concentration (Cmax) |
0.01025; 0.04688; 0.09432; 0.5087; 1.258; 2.092 | — |
| SECONDARY Time to Maximum Plasma Concentration (Tmax) |
111.867; 80.433; 72.364; 100.239; 72.761; 100.247 | — |
Summary
Study BT200-01 is a first in human (FIH) study in male and female normal human volunteers (NHVs) that uses an Integrated Protocol Design. This Phase 1 study will comprise 4 sub-parts: Part A, a single ascending dose (SAD) study; Part B, a multiple ascending dose (MAD) study; Part C, a desmopressin challenge study to explore (i) whether desmopressin could be used as an antidote, and/or (ii) whether desmopressin stimulated vonWillebrand Factor (VWF) release is overcome with increasing BT200 doses; and Part D, a relative bioavailability (BA) study.
The primary objective of this study is to assess the safety and tolerability profile of BT200 in NHVs.
Eligibility Criteria
Inclusion Criteria
- Healthy male or female volunteers, age ≥ 18 years old at screening
- If female, must be post-menopausal or status post hysterectomy
- Able to comprehend and to give informed consent
- Able to cooperate with the Investigator, to comply with the requirements of the study, and to complete the full sequence of protocol-related procedures
Exclusion Criteria
- Clinically significant medical history (including von Willebrand Disease, thrombocytopathy, or any type of bleeding diathesis) or ongoing chronic illness that would jeopardize the safety of the subject or compromise the quality of the data derived from his/her participation in this study
- Clinically relevant abnormal findings on physical examination or clinically relevant laboratory abnormalities
- History of infusion hypersensitivity reactions, significant drug allergy, or anaphylactic reactions
- Substance abuse, mental illness, or any reason that makes it unlikely in the judgment of the Investigator for the subject to be able to comply fully with study procedures
- Use of medication during 2 weeks before the start of the study, which in the judgment of the Investigator may adversely affect the subject's welfare or the integrity of the study's results
- Concurrent treatment with other experimental drugs or participation in another clinical trial with any investigational drug within 30 days or 5 elimination half-lives (whichever is longer) prior to treatment start
Data sourced from ClinicalTrials.gov (NCT04103034). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.