- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05866354
To Evaluate Pharmacokinetics of Tisotumab Vedotin in Chinese Subjects With Metastatic or Recurrent Solid Malignancies
An Open-Label, Phase 1 Trial to Evaluate Pharmacokinetics of Tisotumab Vedotin in Chinese Subjects With Metastatic or Recurrent Solid Malignancies
The goal of this clinical trial is to test in Chinese Subjects with Metastatic or Recurrent Solid Malignancies. The main questions it aims to answer are:
- How is the PK of tisotumab vedotin?
- How is the immunogenicity of tisotumab vedotin?
- How is the safety and tolerability of tisotumab vedotin?
- How is the clinical efficacy of tisotumab vedotin? Participants will receive 2.0 mg/kg tisotumab vedotin (up to a maximum of 200 mg in subjects ≥ 100 kg) as a 30-minute IV infusion 1Q3W with the aim to characterize the PK profiles and to evaluate immunogenicity, safety, and tolerability of tisotumab vedotin in the Chinese population.
Subjects will receive study treatment until disease progression or any other discontinuation criteria are met, whichever occurs first. Subjects will undergo an end of treatment (EOT) visit 30 days (± 5 days) after the last dose of study treatment or within 7 days after treatment discontinuation has been decided, whichever occurs later.
Study Overview
Detailed Description
This is an open-label, phase 1, PK trial of intravenous tisotumab vedotin in Chinese subjects with recurrent or metastatic solid tumors who have failed on previous standard systemic therapy. The screening period will be up to 28 days, after which eligible subjects will receive 2.0 mg/kg tisotumab vedotin (up to a maximum of 200 mg in subjects ≥ 100 kg) as a 30-minute IV infusion 1Q3W with the aim to characterize the PK profiles and to evaluate immunogenicity, safety, and tolerability of tisotumab vedotin in the Chinese population.
Subjects will receive study treatment until disease progression or any other discontinuation criteria are met, whichever occurs first. Subjects will undergo an end of treatment (EOT) visit 30 days (± 5 days) after the last dose of study treatment or within 7 days after treatment discontinuation has been decided, whichever occurs later.
Blood samples for the assessment of tisotumab vedotin concentrations and antidrug antibody (ADA) will be drawn in accordance with the PK and ADA collection schedule. Three different PK analytes will be measured: 1) tisotumab vedotin (conjugated antibody only), 2) total antibody (ie, conjugated and unconjugated antibody), and 3) free MMAE. PK parameters to be estimated will include, but are not limited to, AUC, Cmax, time to maximum concentration (Tmax), apparent terminal half-life (t1/2), and trough concentration (Ctrough).
Safety and tolerability will be evaluated based on TEAEs, clinical safety assessments and clinical laboratory assessments. Ocular AEs are a known safety risk of tisotumab vedotin treatment. Therefore, the eye care plan will be implemented for all subjects enrolled in this trial.
Efficacy assessments will include confirmed ORR assessed by the investigator, primarily based on the enhanced computed tomography (CT) or magnetic resonance imaging (MRI) scans performed at protocol-specified time points. The RECIST v1.1 criteria will be used for response evaluation. After discontinuation of study treatment, tumor assessments may or may not be performed at the discretion of the investigator.
At the end of study (EOS), sponsor will ensure provision of continued tisotumab vedotin to subjects with clinical benefit defined as stable disease (SD) or better, until criteria of treatment discontinuation are met.
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Contact
- Name: Chunye Wang
- Phone Number: +86 13816259037
- Email: Chunye.wang@zailaboratory.com
Study Locations
-
-
Shangdong
-
Jinan, Shangdong, China, 250013
- Jinan Central Hospital
-
Contact:
- Qing Wen, Doctor
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age ≥18 years.
- Must sign an informed consent form (ICF) .
- Must have recurrent or metastatic solid tumors and have failed on previous standard systemic therapy.
- Has Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Has life expectancy of at least 3 months.
- Must demonstrate acceptable screening laboratory values.
- Female subjects must agree not to breastfeed or donate ova. A male subject who is sexually active with a female partner of reproductive potential and has not had a vasectomy must agree to use a barrier method of birth control (eg, condom with spermicide), and all men must also not donate sperm during the trial and for 6 months after receiving the last dose of tisotumab vedotin.
- Any other toxicity caused by previous treatment should have recovered to ≤ CTCAE grade 1 or baseline level, except ≤ CTCAE grade 2 alopecia.
Exclusion Criteria:
- Has clinically significant bleeding issues or risks:
- Has cardiovascular issues or risks:
- Central nervous system (CNS): any history of intracerebral arteriovenous malformation, cerebral aneurysm, or stroke (transient ischemic attack > 1 month prior to screening is allowed).
- Ophthalmological: active ocular surface disease or a history of cicatricial conjunctivitis or inflammatory conditions that predispose to cicatrizing conjunctivitis (eg, Wagner syndrome, atopic keratoconjunctivitis, autoimmune disease affecting the eyes), and subjects with penetrating ocular transplants are ineligible. Cataracts alone is not an exclusion criterion.
- Surgery/procedures: major surgery within 4 weeks or minor surgery within 7 days prior to the first study treatment administration.
- Peripheral neuropathy ≥ grade 2.
- Any prior treatment with MMAE-derived drugs.
- Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy (dose exceeding 10 mg daily of prednisone or equivalent) or any other form of immunosuppressive therapy within 7 days prior to the first dose of tisotumab vedotin.
- Any condition for which, in the opinion of the investigator, participation would not be in the best interest of the subject (eg, compromise well-being) or that could prevent, limit, or confound the protocol-specified assessments.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
PK parameter AUC of tisotumab vedotin
Time Frame: At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
To assess PK of tisotumab vedotin.PK parameters to be estimated will include area under the concentration-time curve (AUC).
|
At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
PK parameter Cmax of tisotumab vedotin
Time Frame: At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
To assess PK of tisotumab vedotin.PK parameters to be estimated will include maximum concentration (Cmax).
|
At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
PK parameter Tmax of tisotumab vedotin
Time Frame: At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
To assess PK of tisotumab vedotin.PK parameters to be estimated will include time to maximum concentration (Tmax).
|
At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
PK parameter t 1/2 of tisotumab vedotin
Time Frame: At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
To assess PK of tisotumab vedotin.PK parameters to be estimated will include apparent terminal half-life (t 1/2).
|
At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
PK parameter C trough of tisotumab vedotin
Time Frame: At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
To assess PK of tisotumab vedotin.PK parameters to be estimated will include trough concentration (C trough).
|
At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Immunogenicity of tisotumab vedotin.
Time Frame: At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
Anti-drug antibodies (ADAs) against tisotumab vedotin.
|
At the end of Cycle 3 (each cycle is 21 days) of the last ongoing patient, about 1 year.
|
Treatment-emergent adverse events (TEAEs) of tisotumab vedotin.
Time Frame: Through study completion, an average of 1 year.
|
A TEAE is defined as a newly occurring or worsening AE from the first dose of study treatment to 30 days after the last dose of study treatment or initiation of new antitumor activities, whichever occurs first.
|
Through study completion, an average of 1 year.
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Objective response rate (ORR) of tisotumab vedotin.
Time Frame: Through study completion, an average of 1 year.
|
Confirmed objective response rate (ORR) assessed by the investigator per the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.
|
Through study completion, an average of 1 year.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rutie Yin, Dr, West China Second University Hospital
- Principal Investigator: Bingzhong Zhang, Dr, Sun Yat-sen Memorial Hospital,Sun Yat-sen University
- Principal Investigator: Qing Wen, Dr, Jinan Central Hospital
- Principal Investigator: Meili Sun, Dr, Jinan Central Hospital
- Principal Investigator: Jianhua Shi, Dr, Linyi Cancer Hospital
- Principal Investigator: Dongqing Lv, Dr, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University
- Principal Investigator: Tienan Yi, Dr, Xiangyang Central Hospital
- Principal Investigator: Guiling Li, Dr, Union Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ZL-1309-002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Solid Malignancies
-
National University Hospital, SingaporeRecruitingMetastatic Solid Malignancies | Advance Solid MalignanciesSingapore
-
AHS Cancer Control AlbertaCross Cancer InstituteWithdrawnMetastatic Solid Malignancies | Locally Advanced Solid MalignanciesCanada
-
Kiromic, Inc.TerminatedCancer | Progressive Solid Malignancies | Refractory Solid MalignanciesUnited States
-
University Hospital, Clermont-FerrandAmgenUnknown
-
Zhuhai Yufan Biotechnologies Co., LtdRecruitingAdvanced Solid Tumor | Advanced Solid MalignanciesChina
-
Zhuhai Yufan Biotechnologies Co., LtdRecruitingAdvanced Solid Tumor | Advanced Solid MalignanciesUnited States
-
AstraZenecaQuintiles, Inc.CompletedSolid MalignanciesUnited Kingdom
-
University Hospital, Clermont-FerrandAmgenTerminatedSolid Malignancies
-
AstraZenecaCompletedCancer | Solid Tumors | Advanced Solid MalignanciesJapan
-
AstraZenecaTerminatedCancer | Solid Tumors | Advanced Solid MalignanciesJapan
Clinical Trials on Tisotumab Vedotin
-
Seagen Inc.GenmabCompletedOvarian Cancer | Fallopian Tube Cancer | Peritoneal CancerUnited States, Spain, Belgium, Denmark, Ireland, Italy
-
Seagen Inc.Gynecologic Oncology Group; European Network of Gynaecological Oncological... and other collaboratorsCompletedCervical CancerBelgium, Spain, United States, Denmark, Italy, Germany, Czechia, Sweden
-
GenmabSeagen Inc.Completed
-
Seagen Inc.GenmabCompletedProstate Cancer | Squamous Cell Carcinoma of the Head and Neck | Bladder Cancer | Cervix Cancer | Lung Cancer, Nonsmall Cell | Ovary Cancer | Esophagus Cancer | Endometrium CancerUnited States, United Kingdom
-
Seagen Inc.GenmabCompletedBladder Cancer | Cervix Cancer | Ovary Cancer | Esophagus Cancer | Endometrium Cancer | Prostate Cancer (CRPC) | Lung Cancer (NSCLC)United States, United Kingdom, Belgium, Hungary, Denmark
-
Seagen Inc.GenmabCompletedBladder Cancer | Cervix Cancer | Ovary Cancer | Esophagus Cancer | Squamous Cell Carcinoma of the Head and Neck (SCCHN) | Endometrium Cancer | Prostate Cancer (CRPC) | Lung Cancer(NSCLC)United States, Belgium, United Kingdom, Denmark, Sweden
-
Seagen Inc.Merck Sharp & Dohme LLC; GenmabRecruitingCarcinoma, Non-Small-Cell Lung | Colorectal Neoplasms | Exocrine Pancreatic Cancer | Carcinoma, Squamous Cell of Head and NeckUnited States, Canada, France, Germany, Italy, Spain, United Kingdom, Puerto Rico
-
Seagen Inc.Merck Sharp & Dohme LLC; GOG Foundation; European Network of Gynaecological Oncological... and other collaboratorsActive, not recruitingCervical CancerUnited States, Belgium, Netherlands, Czechia, Spain, Turkey, Ireland, United Kingdom, Italy, Denmark
-
Seagen Inc.GenmabRecruitingCervical CancerUnited States, Canada, Japan, Austria, Belgium, China, France, Korea, Republic of, Netherlands, Singapore, Spain, United Kingdom, Argentina, Brazil, Germany, Italy, Norway, Peru, Poland, Finland, Denmark, Ireland, Czechia, Hungary, Taiwan, Swed... and more
-
Tianjin Medical University Second HospitalRecruitingHer2 Overexpressing High-Risk Non-Muscle Invasive Bladder Urothelial CarcinomaChina