Evaluate the Safety, Tolerability, Pharmacokinetics, & Preliminary

See also
Status	Clinical Trial	Phase
Recruiting	`NCT04277637` - Study of Bcl-2 Inhibitor BGB-11417 in Participants With Mature B-Cell Malignancies	Phase 1
Active, not recruiting	`NCT04883957` - Study of BGB-11417 in Adult Participants With Mature B-cell Malignancies	Phase 1
Active, not recruiting	`NCT04172246` - Study of Zanubrutinib in Japanese Participants With B-Cell Malignancies	Phase 1/Phase 2

See also

Status

Clinical Trial

Phase

Recruiting

NCT04277637 - Study of Bcl-2 Inhibitor BGB-11417 in Participants With Mature B-Cell Malignancies

Phase 1

Active, not recruiting

NCT04883957 - Study of BGB-11417 in Adult Participants With Mature B-cell Malignancies

Phase 1

Active, not recruiting

NCT04172246 - Study of Zanubrutinib in Japanese Participants With B-Cell Malignancies

Phase 1/Phase 2

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT06351527
Study type	Interventional
Source	InnoCare Pharma Inc.
Contact	Alexia Lu
Phone	010-66609745
Email	CO_HGRAC@innocarepharma.com
Status	Not yet recruiting
Phase	Phase 1
Start date	April 25, 2024
Completion date	October 25, 2027

Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of ICP-248 in Mature B-cell Malignancies

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms