TriangleNCT03913741 · CITED IN SOURCE DOCUMENTS
A Trial of Tisotumab Vedotin in Japanese Subjects With Advanced Solid Malignancies
An NCI or FDA source cites this study. A citation does not establish that it applies to an individual diagnosis.
- Phase
- PHASE1, PHASE2
- Status at capture
- COMPLETED
- Registry last update
- 2022-06-23
Open Label Phase 1/2 Trial of Tisotumab Vedotin in Japanese Subjects with Advanced Solid Malignancies
Open the original ClinicalTrials.gov record → · Download preserved record
What did the study report?
Outcomes, safety and baseline populations are separate source sections. Quality-of-life measures appear under their original outcome titles.
No posted result sections were captured. Registered plans do not establish that a treatment works.
Who could take part
- eligibility Criteria
- 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
- healthy Volunteers
- false
- minimum Age
- 20 Years
- sex
- ALL
- std Ages
- ADULT
- OLDER_ADULT
Treatment arms and interventions
- arm Groups
- description
- Open label, single arm trial where tisotumab vedotin will be administered
- intervention Names
- Drug: tisotumab vedotin
- label
- Experimental tisotumab vedotin
- type
- EXPERIMENTAL
- interventions
- arm Group Labels
- Experimental tisotumab vedotin
- description
- 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
- name
- tisotumab vedotin
- type
- DRUG
Study design
- allocation
- NA
- intervention Model
- SINGLE_GROUP
- intervention Model Description
- Single Group assignment
- masking Info
- masking
- NONE
- primary Purpose
- TREATMENT
Enrollment
- count
- 23
- type
- ACTUAL
Registered outcome plans (not posted results)
- primary Outcomes
- measure
- Dose Escalation and Dose Expansion: Incidence of drug-related Adverse Events (AEs) and Serious Adverse Events (SAEs) by CTCAE v5.0 [Safety]
- time Frame
- Throughout the trial - until 90 days after last dose of tisotumab vedotin
- measure
- 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]
- time Frame
- Throughout the trial - until 90 days after last dose of tisotumab vedotin
- measure
- Dose Escalation: maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D) of tisotumab vedotin
- time Frame
- Up to 21 days after the first dose of tisotumab vedotin (each cycle is 21 days)
- measure
- Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin: Maximum concentration (Cmax) after dosing
- time Frame
- Up to approximately 42 days after initial dose of tisotumab vedotin
- measure
- 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))
- time Frame
- Up to approximately 42 days after initial dose of tisotumab vedotin
- measure
- Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin : Rate at which the drug is removed from the body (CL)
- time Frame
- Up to approximately 42 days after initial dose of tisotumab vedotin
- measure
- Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin: Elimination half-life of the drug (T½)
- time Frame
- Up to approximately 42 days after initial dose of tisotumab vedotin
- measure
- Dose Escalation and Dose Expansion Pharmacokinetics of tisotumab vedotin: Time after dosing at which the maximum drug concentration was observed (Tmax)
- time Frame
- Up to approximately 42 days after initial dose of tisotumab vedotin
- description
- Summarized by descriptive statistics by trial part and dose
- measure
- Dose Escalation and Dose Expansion: Assess immunogenicity of tisotumab vedotin by measuring and assessing Anti-drug Antibody (ADA)
- time Frame
- Throughout and at the end of trial (up to 90 days after last dose of tisotumab vedotin)
- secondary Outcomes
- description
- ORR defined as the percentage of participants with a confirmed complete response (CR) or partial response (PR)
- measure
- Dose Escalation and Dose Expansion: Evaluate antitumor activity of tisotumab vedotin by assessing Objective Response Rate (ORR) (based on RECIST 1.1)
- time Frame
- Up to approximately 6 months after the first dose of tisotumab vedotin
- description
- 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.
- measure
- Dose Escalation and Dose Expansion: Evaluate antitumor activity of tisotumab vedotin by assessing Duration of Response (DOR) (based on RECIST 1.1)
- time Frame
- Up to approximately 6 months after the first dose of tisotumab vedotin
- description
- TTR for a responder is defined as the time from the start of treatment with study drug to the first objective tumor response observed.
- measure
- Dose Escalation and Dose Expansion: Evaluate antitumor activity of tisotumab vedotin by assessing Time to Response (TTR) (based on RECIST 1.1)
- time Frame
- Up to approximately 6 months after the first dose of tisotumab vedotin
Full study description
- 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
Source references
- references
- citation
- Yonemori K, Kuboki Y, Hasegawa K, Iwata T, Kato H, Takehara K, Hirashima Y, Kato H, Passey C, Buchbjerg JK, Harris JR, Andreassen CM, Nicacio L, Soumaoro I, Fujiwara K. Tisotumab vedotin in Japanese patients with recurrent/metastatic cervical cancer: Results from the innovaTV 206 study. Cancer Sci. 2022 Aug;113(8):2788-2797. doi: 10.1111/cas.15443. Epub 2022 Jun 15.
- pmid
- 35633184
- type
- RESULT
Source notices and limitations
Discovery and provenance
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- occurrences
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- ntravenously every 3 weeks in innovaTV 301, innovaTV 204, innovaTV 201 (NCT02001623), innovaTV 202 (NCT02552121), innovaTV 203 (NCT03245736), and innovaTV 206 (NCT03913741). The median duration of treatment with TIVDAK was 3.7 months (range: 0.4-40.2). In this pooled safety population, the most common (≥25%) adverse reactions, in
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Preserved source evidence · Not medical advice