BIIB021
DrugDosage, frequency (once daily), and duration as specified in protocol. This dosing arm is currently on hold.
Other names: CNF2024
NCT Number: NCT00618735
The purpose of the study is to see if daily and twice daily administration of BIIB021 is tolerated in patients with advanced solid tumors.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 1
Research Site, Encinitas, California, United States
Heat shock protein 90 (HSP90) inhibitors are anticipated to have clinical activity in solid tumors because Hsp90 is required for the folding, activation, and assembly of many proteins involved in cancer cell survival, proliferation, and metastasis. The maximum tolerated dose (MTX) for BIIB021 administered twice weekly in a phase I study in subjects with advanced solid tumors have been defined at 600mg. It is now reasonable from a safety perspective and desirable from a pharmacokinetic perspective to evaluate more frequent dosing intervals in solid tumors with the goal of providing more sustained and completed inhibition of Hsp90.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Subjects with histologically or cytologically confirmed solid tumor who have failed or refused standard therapies or for which no approved therapy is available.
Age greater than or equal to 18 years at the time of informed consent. ECOG performance status of less than or equal to 2. Lab values consistent with adequate renal, hepatic, and bone marrow functions.
Exclusion criteria
Prior antitumor therapies, including prior experimental agents or approved antitumor small molecules and biologics within 28 days and all associated toxicities resolved to eligibility levels.
Subjects with known brain metastases. Concurrent severe or uncontrolled medical disease. Must utilize effective contraception.
Dosage, frequency (once daily), and duration as specified in protocol. This dosing arm is currently on hold.
Other names: CNF2024
Time frame: As specified in protocol
Time frame: As specified in protocol
Time frame: As specified in protocol
Biogen
Industry
A Phase 1, Multicenter, Open-Label, Dose-Escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of BIIB021 Administered Once or Twice Daily to Subjects With Advanced Solid Tumors
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04826341
Advanced Solid Tumors, HRD Cancer
Bethesda, Maryland, United States
View Trial DetailsNCT05740202
Advanced Solid Tumors
Tianjin, Tianjin Municipality, China
View Trial DetailsNCT06242691
Advanced Solid Tumors
Louisville, Kentucky, United States
View Trial DetailsNCT06235983
Advanced Solid Tumors
Changchun, Jilin, China
View Trial Details