Solid Tumor
Conditions
Keywords
tisotumab vedotin, cervical cancer
Brief summary
Open Label Phase 1/2 Trial of Tisotumab Vedotin in Japanese Subjects with Advanced Solid Malignancies
Detailed description
Part 1 of this trial will determine the maximum tolerated dose (MTD) and/or the recommended Phase 2 dose (RP2D) and the safety profile of tisotumab vedotin in subjects with solid malignancies. Part 2 of this trial will enroll subjects with cervical cancer to provide further data on the safety, tolerability, PK and anti-tumor activity
Interventions
Tisotumab vedotin will be administered intravenously once every 21 days. The dose levels will be determined by the starting dose and the escalation steps taken in the trial
Sponsors
Seagen Inc.
Genmab
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Single Group assignment
Eligibility
Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No
Inclusion criteria
(Main): * PART 1 ONLY: Subjects with locally advanced or metastatic solid tumors, who have experienced disease progression while on standard therapy or are intolerant of, or not eligible for, standard therapy. * PART 2 ONLY: Subjects with extra-pelvic metastatic or recurrent cervical cancer including squamous cell, adenocarcinoma or adenosquamous histology who have experienced disease progressed on standard of care chemotherapy in combination with bevacizumab, if eligible. Patients must not have received more than 2 prior systemic treatment regimens for recurrent or metastatic cervical disease. * Measurable disease according to RECIST v1.1 * Must be at least 20 years of age on the day of signing informed consent * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 * Is not pregnant, breastfeeding, or expecting to conceive children within the projected duration of the trial and for at least 6 months after the last trial treatment administration * Women of childbearing potential must agree to use adequate contraception during and for 6 months after the last dose of trial treatment administration * A man who is sexually active with a WOCBP and has not had a vasectomy must agree to use a barrier method of birth control (Part 1 only) * Must provide signed informed consent before any trial-related activity is carried out.
Exclusion criteria
(Main): * PART 2 ONLY: Clinically relevant bilateral hydronephrosis which cannot be alleviated by ureteral stents or percutaneous drainage. * Known past or current coagulation defects leading to an increased risk of bleeding. * Ongoing major bleeding. * Has an active ocular surface disease at baseline. Subjects with prior history of cicatricial conjunctivitis are ineligible
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Dose Escalation and Dose Expansion: Assess immunogenicity of tisotumab vedotin by measuring and assessing Anti-drug Antibody (ADA) | Throughout and at the end of trial (up to 90 days after last dose of tisotumab vedotin) | Summarized by descriptive statistics by trial part and dose |
| Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin : Rate at which the drug is removed from the body (CL) | Up to approximately 42 days after initial dose of tisotumab vedotin | — |
| Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin: Elimination half-life of the drug (T½) | Up to approximately 42 days after initial dose of tisotumab vedotin | — |
| Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin: Time after dosing at which the maximum drug concentration was observed (Tmax) | Up to approximately 42 days after initial dose of tisotumab vedotin | — |
| Dose Escalation and Dose Expansion: Incidence of drug-related Adverse Events (AEs) and Serious Adverse Events (SAEs) by CTCAE v5.0 [Safety] | Throughout the trial - until 90 days after last dose of tisotumab vedotin | — |
| Dose Escalation and Dose Expansion: Incidence of Dose Limiting Toxicities (DLTs), AEs, SAEs, adverse events leading to discontinuation, deaths and clinical laboratory test abnormalities [Tolerability] | Throughout the trial - until 90 days after last dose of tisotumab vedotin | — |
| Dose Escalation: maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D) of tisotumab vedotin | Up to 21 days after the first dose of tisotumab vedotin (each cycle is 21 days) | — |
| Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin: Maximum concentration (Cmax) after dosing | Up to approximately 42 days after initial dose of tisotumab vedotin | — |
| Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin: Area under the plasma concentration-time curve from time 0 to the last measurable concentration (AUC(0-t)) | Up to approximately 42 days after initial dose of tisotumab vedotin | — |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Dose Escalation and Dose Expansion: Evaluate antitumor activity of tisotumab vedotin by assessing Duration of Response (DOR) (based on RECIST 1.1) | Up to approximately 6 months after the first dose of tisotumab vedotin | The DOR for a responder is defined as the time from the participant's initial objective response to the first date of either disease progression or death, whichever occurs first. |
| Dose Escalation and Dose Expansion: Evaluate antitumor activity of tisotumab vedotin by assessing Time to Response (TTR) (based on RECIST 1.1) | Up to approximately 6 months after the first dose of tisotumab vedotin | TTR for a responder is defined as the time from the start of treatment with study drug to the first objective tumor response observed. |
| Dose Escalation and Dose Expansion: Evaluate antitumor activity of tisotumab vedotin by assessing Objective Response Rate (ORR) (based on RECIST 1.1) | Up to approximately 6 months after the first dose of tisotumab vedotin | ORR defined as the percentage of participants with a confirmed complete response (CR) or partial response (PR) |
Countries
Japan
Outcome results
None listed