This research is designed to determine if experimental treatment with Antibody-drug conjugate, AZD5335, alone, or in combination with anti-cancer agents is safe, tolerable, and has anti-cancer activity in patients with advanced tumors
This study is a Phase I/IIa modular, open-label, multi-center study of AZD5335 administered either as monotherapy or in combination with other anti-cancer agents in participants with advanced solid malignancies
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
602
Number of participants with adverse events/serious adverse events
Number of participants with incidence of adverse events and with serious adverse events including changes from baseline in laboratory parameters, vital signs, ECGs, and physical examination.
Time frame: From time of Informed Consent to 30 days post last dose.
The number of participants with dose limiting toxicity(DLT), as defined in the protocol
A DLT is defined as any ≥ Grade 3 treatment-emergent AE that occurs during the DLT evaluation period, not attributable to the underlying disease or extraneous causes (as defined in the protocol)
Time frame: From the first dose of torvu-sam on Cycle 1 Day 1 up to and including the planned end of Cycle 1 (At the end of 21 days)
Objective Response Rate (ORR)
The percentage of participants with a confirmed CR or PR according to RECIST v1.1 criteria.
Time frame: From time of Informed Consent to progressive disease or withdrawal of consent.(approx 2 years)
Duration of Response (DoR)
The time from the date of first response until date of disease progression or death in the absence of disease progression.
Time frame: From the first documented response to confirmed progression or death in the absence of disease progression.(approx 2 years)
Disease Control Rate (DCR)
The percentage of participants who have a best objective response of confirmed CR or PR or who have SD for at least 15 weeks after start of treatment (to allow for an early assessment within the assessment window).
Time frame: From time of Informed Consent until progression.(approx 15 weeks)
Progression free Survival (PFS)
AstraZeneca Clinical Study Information Center
CONTACT
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IV Alkylating agent
Oral PARP inhibitor
IV Biologic
Research Site
Duarte, California, United States
RECRUITINGResearch Site
Irvine, California, United States
RECRUITINGResearch Site
La Jolla, California, United States
WITHDRAWNResearch Site
Aurora, Colorado, United States
RECRUITINGResearch Site
Louisville, Kentucky, United States
TERMINATEDResearch Site
Boston, Massachusetts, United States
RECRUITINGResearch Site
Detroit, Michigan, United States
RECRUITINGResearch Site
Columbus, Ohio, United States
RECRUITINGResearch Site
Portland, Oregon, United States
RECRUITINGResearch Site
Providence, Rhode Island, United States
RECRUITING...and 50 more locations
Progression-free survival is defined as the time from the start of treatment until the date of objective disease progression or death (by any cause in the absence of progression), regardless of whether the participant withdraws from assigned therapy or receives another anti-cancer therapy prior to progression. Participants who have not progressed or died at the time of analysis will be censored at the time of the latest date of assessment from their last evaluable RECIST v1.1 assessment
Time frame: From time of first dose of torvu-sam or anti-cancer study agent until the date of objective disease progression or death (by any cause in the absence of progression) (approx 2 years)
Overall Survival (OS)
The time until death due to any cause.
Time frame: From time of first dose of torvu-sam or anti-cancer study agent until death due to any cause (approx 2 years)
Module 1: Pharmacokinetics of torvu-sam
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approx 12 weeks) through 30-day follow-up
Module 1: Pharmacokinetics of torvu-sam: Area Under the concentration-time curve(AUC)
Area under the plasma concentration-time curve
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
Module 1: Pharmacokinetics of torvu-sam: Maximum plasma concentration of the study drug (Cmax)
Maximum observed plasma concentration of the study drug
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
Module 1: Pharmacokinetics of torvu-sam: Time to maximum plasma concentration of the study drug (T-max)
Time to maximum observed plasma concentration of the study drug
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
Module 1: Pharmacokinetics of torvu-sam: Clearance
A pharmacokinetic measurement of the volume of plasma from which the study drug is completely removed per unit time.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
Module 1: Pharmacokinetics of torvu-sam: Terminal elimination half-life (t 1/2)
Terminal elimination half-life.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
Module 1: To investigate baseline and on treatment changes in target expression.
The clinical activity by baseline and on-treatment changes in tumor target expression.
Time frame: Baseline and predicted intervals throughout the administration of torvu-sam (approx 2 years)
Module 2: Pharmacokinetics of torvu-sam and saruparib when given in combination.
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and saruparib (approx 12 weeks) through 30-day follow-up
Module 3: Pharmacokinetics of torvu-sam and bevaczizumab when given in combination.
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and bevacizumab (approx 12 weeks) through 30-day follow-up
Module 4: Pharmacokinetics of torvu-sam and carboplatin (+/- bevacizumab) when given in combination.
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and carboplatin (+/- bevacizumab) (approx 12 weeks) through 30-day follow-up
Module 5: Pharmacokinetics of torvu-sam and palacaparib (+/- bevacizumab) when given in combination.
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and palacaparib (+/- bevacizumab) (approx 12 weeks) through 30-day follow-up
Module 6: Pharmacokinetics of torvu-sam and pembrolizumab (+/- palacaparib) when given in combination.
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and pembrolizumab (+/- palacaparib).(approx 12 weeks) through 90-day follow-up
Module 2, 3, 4, 5, and 6: Area Under the concentration-time curve (AUC)
Area under the plasma concentration-time curve
Time frame: At predefined intervals throughout the treatment period (approximately 12 weeks)
Module 2, 3, 4, 5, and 6: Maximum plasma concentration of the study drug (Cmax)
Maximum observed plasma concentration of the study drug
Time frame: At predefined intervals throughout the treatment period (approximately 12 weeks)
Module 2, 3, 4, 5, and 6: Time to maximum plasma concentration of the study drug (T-max)
Time to maximum observed plasma concentration of the study drug
Time frame: At predefined intervals throughout the treatment period (approximately 12 weeks)
Module 2, 3, 4, 5, and 6: Clearance
A pharmacokinetic measurement of the volume of plasma from which the study drug is completely removed per unit time.
Time frame: At predefined intervals throughout the treatment period (approximately 12 weeks)
Module 2, 3, 4, 5, and 6: Terminal elimination half-life (t 1/2)
Terminal elimination half-life.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks)
Immunogenicity of torvu-sam
The number and percentage of participants who develop ADAs.
Time frame: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approx 2 years) through 30-day follow-up