Non-small Cell Lung CancerPhase 1NCT04254107
A Safety Study of SEA-TGT (SGN-TGT) in Advanced Cancer
A Phase 1 study testing SEA-TGT, sasanlimab and brentuximab vedotin in people with Non-small Cell Lung Cancer and Gastric Carcinoma, run by Seagen Inc. at 36 sites in 6 countries.
Trial summary
This trial will look at a drug called SEA-TGT (also known as SGN-TGT) to find out whether it is safe for patients with solid tumors and lymphomas. It will study SEA-TGT to find out what its side effects are. A side effect is anything the drug does besides treating cancer. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Non-small Cell Lung Cancer, Gastric Carcinoma, Gastroesophageal Junction Carcinoma
- What is being tested?
- SEA-TGT, sasanlimab and brentuximab vedotin
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 133 participants
- Where
- 36 sitesin 6 countries
- Study dates
- 29 May 2020to 1 Dec 2023
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Monotherapy Inclusion Criteria (Parts A and B)
- Histologically- or cytologically-confirmed advanced or metastatic malignancy, defined as:
- One of the following tumor types:
- Unresectable locally-advanced or metastatic non-small cell lung cancer (NSCLC), gastric/gastroesophageal (GE) junction carcinoma, cutaneous melanoma, head and neck squamous cell carcinoma (HNSCC), bladder cancer, cervical cancer, ovarian cancer, or triple negative breast cancer (TNBC)
- Lymphomas, including:
- cHL
- Diffuse large B-cell lymphoma (DLBCL)
- Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS)
- Lymphoma: Participants should have disease progression on or after treatment with standard therapies expected to provide benefit in the judgement of the investigator.
- cHL: Participants must have received at least 3 prior systemic therapies. Participants should have had disease recurrence or progression following brentuximab vedotin therapy or have been ineligible to receive brentuximab vedotin. Participants who have not received autologous stem cell transplant (SCT) must have refused or been deemed ineligible. Participants should have received or not be eligible to have received an anti-PD-1 agent.
- DLBCL: Participants must have received at least 2 prior systemic chemo-immunotherapy regimens, including an anti-CD20 agent and combination chemotherapy. Unless clinically contraindicated, participants should have had disease that has relapsed after or be refractory to intensive salvage chemotherapy, including autologous SCT.
- PTCL-NOS: Participants must have had at least 1 prior systemic therapy. Participants must have received or have been ineligible to receive the combination of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) or CHOP-like therapy. Participants with CD30-positive disease must have received or be ineligible to receive brentuximab vedotin. Participants must have also received intensive salvage therapy (defined as combination chemotherapy ± autologous SCT) unless they refused or were deemed ineligible.
- Measurable disease defined as:
- Solid tumors: Measurable disease according to RECIST V1.1
- Lymphomas: Fluorodeoxyglucose (FDG)-avid disease by positron emission tomography (PET) and measurable disease of ≥15 mm in the greatest transverse diameter by computed tomography (CT) scan, as assessed by the site radiologist.
- A representative archival tumor tissue sample should be available as follows: Participants must provide archived tumor tissue, if available, from the most recent biopsy (less than or equal to [≤] 12 months from screening). If archived tissue is not available, a fresh baseline tumor biopsy will be requested for any participant enrolled in Part B whose tumors are considered accessible and appropriate in the opinion of the investigator.
- ECOG Performance Status score of 0 or 1
Combination Inclusion Criteria (Part C)
- ECOG Performance Status score of 0 or 1
- NSCLC: histological or cytological confirmed metastatic disease. Participants must have received no prior anti-PD-1/PD-L1 therapy allowed.
- HNSCC: histological or cytological confirmed metastatic disease. Participants must have received no prior exposure to anti-PD-1/PD-L1 therapy.
- Cutaneous Melanoma: histological or cytological confirmed metastatic disease. Participants must not have received anti-PD-1/PD-L1 targeted therapy.
- Measurable disease by CT or magnetic resonance imaging (MRI) as defined by RECIST V1.1
- Participants must provide archival tumor tissue from the most recent biopsy (≤12 months from screening). If archival tissue is not available, a fresh baseline tumor biopsy that has not been previously irradiated is required for any participant whose tumors are considered accessible and appropriate in the opinion of the investigator.
Combination Inclusion Criteria (Part D)
- Histologically- or cytologically-confirmed advanced stage cHL
- cHL patients that have failed standard of care for R/R disease including prior treatment with BV.
- FDG PET emission tomography avid and bidimensional measurable disease of at least 1.5 cm in longest axis as documented by radiographic technique
- ECOG performance status of ≤ 2
- Participants are required to have tumor tissue, if available, from the most recent biopsy (≤12 months from screening) prior to start of study treatment. If archival tissue is not available, a fresh screening tumor biopsy is required for any participant whose tumors are considered accessible and appropriate in the opinion of the investigator.
Monotherapy Exclusion Criteria (Parts A and B)
- History of another malignancy within 2 years before the first dose of study drug, or any evidence of residual disease from a previously diagnosed malignancy. Exceptions are malignancies with a negligible risk of metastasis or death.
- Chemotherapy, radiotherapy, biologics, and/or other antitumor treatment that has not been completed before the first dose of study drug within the timeframe as follows:
- Chemotherapy, small molecule inhibitors, radiation, and/or other investigational anticancer agents (excluding investigational monoclonal antibodies): 2 weeks
- Palliative radiotherapy (≤2 weeks of radiotherapy to non-central nervous system [CNS] disease): ≤7 days prior to start of SEA-TGT
- Immune-checkpoint inhibitors: 4 weeks
- Monoclonal antibodies, antibody-drug conjugates (ADC), or radioimmunoconjugates: 4 weeks (2 weeks with documented disease progression)
- T-cell or other cell-based therapies: 12 weeks
- Known CNS metastases
- Participants with a history of CNS metastases are allowed if they have undergone treatment for the CNS disease, symptoms have resolved, and steroids have been discontinued.
- Leptomeningeal involvement by malignant disease is excluded regardless of prior treatment.
- Previous allogeneic stem cell transplant (SCT). Participants with prior autologous SCT may be eligible if they are >100 days from autologous SCT and fulfill all other inclusion criteria.
- Prior use of any anti-TIGIT mAb.
- Participants with a condition requiring systemic treatment with either corticosteroids (greater than [>]10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days of enrollment. Inhaled or topical steroids and adrenal replacement steroid doses >10 mg daily prednisone or equivalents are permitted in the absence of active immune disease.
- Known hypersensitivity to any excipient contained in the drug formulation of SEA-TGT
Combination Exclusion Criteria (Part C)
- History of another malignancy within 2 years before the first dose of study drug, or any evidence of residual disease from a previously diagnosed malignancy. Exceptions are malignancies with a negligible risk of metastasis or death.
- Active, non-infectious pneumonitis, pulmonary fibrosis, or known history of immune mediated pneumonitis.
- Previous therapy with an anti-PD-1 or anti-PD-L1 inhibitor.
- Chemotherapy, radiotherapy, biologics, and/or other antitumor treatment that has not been completed before the first dose of study drug within the timeframe as follows:
- Chemotherapy, small molecule inhibitors, radiation, and/or other investigational anticancer agents (excluding investigational monoclonal antibodies): 2 weeks
- Palliative radiotherapy (≤2 weeks of radiotherapy to non-CNS disease): ≤7 days prior to start of SEA-TGT.
- Immune-checkpoint inhibitors: 4 weeks
- Monoclonal antibodies, ADC, or radioimmunoconjugates: 4 weeks (2 weeks with documented disease progression)
- T-cell or other cell-based therapies: 12 weeks
- Known active CNS metastases.
- Participants with a history of CNS metastases are allowed if they have undergone treatment for the CNS disease, symptoms have resolved, and steroids have been discontinued.
- Leptomeningeal involvement by malignant disease is excluded regardless of prior treatment.
- Known hypersensitivity to any excipient contained in the drug formulation of SEA-TGT or sasanlimab
- Participants with active known or suspected autoimmune disease or significant autoimmune-related toxicity from prior immuno-oncology-based therapy (prior autoimmune colitis, pneumonitis, transaminitis); Participants with vitiligo, controlled type 1 diabetes mellitus, residual hypothyroidism requiring hormone replacement, or conditions not expected to recur in the absence of an external trigger are permitted to enroll.
- History of interstitial lung disease
- Participants with a condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days of enrollment. Inhaled or topical steroids and adrenal replacement steroid doses >10 mg daily prednisone or equivalents are permitted in the absence of active immune disease.
- Prior use of any anti-TIGIT mAb
Combination Exclusion Criteria (Part D)
- History of another malignancy within 2 years before the first dose of study drug, or any evidence of residual disease from a previously diagnosed malignancy. Exceptions are malignancies with a negligible risk of metastasis or death.
- Chemotherapy, radiotherapy, biologics, and/or other antitumor treatment that has not been completed before the first dose of study drug within the timeframe as follows:
- Chemotherapy, small molecule inhibitors, radiation, and/or other investigational anticancer agents (excluding investigational monoclonal antibodies): 2 weeks
- Palliative radiotherapy (≤2 weeks of radiotherapy to CNS disease): ≤7 days prior to start of SEA-TGT
- Immune-checkpoint inhibitors: 4 weeks
- Monoclonal antibodies, ADC (except brentuximab vedotin), or radioimmunoconjugates: 4 weeks (2 weeks with documented disease progression)
- T-cell or other cell-based therapies: 12 weeks
- Known active CNS involvement by lymphoma
- Previous allogeneic SCT. Participants with prior autologous SCT may be eligible if they are >100 days from autologous SCT and fulfill all other inclusion criteria.
- Prior use of any anti-TIGIT mAb.
- Participants with a condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days of enrollment. Inhaled or topical steroids and adrenal replacement steroid doses >10 mg daily prednisone or equivalents are permitted in the absence of active immune disease.
Trial locations and contacts
36 sites in 6 countries.
36 sites in 6 countries
United States26 sites
University of Michigan Comprehensive Cancer Center
Ann Arbor, Michigan, 48109
Texas Oncology - Austin Midtown
Austin, Texas, 78705
Johns Hopkins Medical Center
Baltimore, Maryland, 21287
University of Alabama at Birmingham
Birmingham, Alabama, 35249
Oncology and Hematology Assoc of SW VA DBA Blue Ridge Cancer Care
Blacksburg, Virginia, 24060
University of Cincinnati Cancer Institute
Cincinnati, Ohio, 45219
Texas Oncology - Baylor Sammons Cancer Center
Dallas, Texas, 75246
City of Hope
Duarte, California, 91010-3000
Virginia Cancer Specialists, PC
Fairfax, Virginia, 22031
MD Anderson Cancer Center / University of Texas
Houston, Texas, 77030
University of Mississippi Medical Center
Jackson, Mississippi, 39216
California Research Institute
Los Angeles, California, 90027
Carbone Cancer Center / University of Wisconsin
Madison, Wisconsin, 53792
Minnesota Oncology Hematology P.A.
Minneapolis, Minnesota, 55404
Vanderbilt University Medical Center
Nashville, Tennessee, 37204
Yale Cancer Center
New Haven, Connecticut, 06520
Weill Cornell Medicine
New York, New York, 10021
Memorial Sloan Kettering Cancer Center
New York, New York, 10065
University of Pittsburgh Medical Center (UPMC)/Hillman Cancer Center
Pittsburgh, Pennsylvania, 15232
Providence Portland Medical Center
Portland, Oregon, 97213
Mayo Clinic Rochester
Rochester, Minnesota, 55905
Maryland Oncology Hematology, P.A.
Rockville, Maryland, 20850
University of California, San Francisco | HDFCCC - Hematopoietic Malignancies
San Francisco, California, 94134
Arizona Oncology Associates, PC - HOPE
Tucson, Arizona, 85710
Texas Oncology - Northeast Texas
Tyler, Texas, 75702
Wake Forest Baptist Medical Center / Wake Forest University
Winston-Salem, North Carolina, 27157
Spain3 sites
Hospital Universitari Vall d'Hebron
Barcelona, Other, 08035
L'Institut Catala d'Oncologia
L'Hospitalet de Llobregat, Other, 08908
HM Centro Integral Oncologico Clara Campal
Madrid, Other, 28050
Canada2 sites
University of Alberta / Cross Cancer Institute
Edmonton, Alberta, T6G 1Z2
University Health Network, Princess Margaret Hospital
Toronto, Other, M5G 2C1
Italy2 sites
Istituto Europeo di Oncologia
Milan, Other, 20132
Policlinico Universitario Agostino Gemelli
Rome, Other, 00168
United Kingdom2 sites
Sarah Cannon Research Institute UK
London, Other, W1G 6AD
The Royal Marsden Hospital (Surrey)
Sutton, Other, SM2 5PT
About this study
Official title: A Phase 1 Study of SEA-TGT (SGN-TGT) in Subjects With Advanced Malignancies
This trial will look at a drug called SEA-TGT (also known as SGN-TGT) to find out whether it is safe for patients with solid tumors and lymphomas. It will study SEA-TGT to find out what its side effects are. A side effect is anything the drug does besides treating cancer. It will also study whether SEA-TGT works to treat solid tumors and lymphomas.
The study will have four parts. Part A of the study will find out how much SEA-TGT should be given to patients. Part B will use the dose found in Part A to find out how safe SEA-TGT is and if it works to treat solid tumors and lymphomas. Part C will study how well SEA-TGT with sasanlimab works to treat solid tumors. Part D will study how well SEA-TGT with brentuximab vedotin works to treat classical Hodgkin lymphoma (cHL).
- Conditions
- Non-small Cell Lung Cancer, Gastric Carcinoma, Gastroesophageal Junction Carcinoma, Classical Hodgkin Lymphoma, Diffuse Large B-cell Lymphoma, Peripheral T-cell Lymphoma
- Being tested
- SEA-TGT, sasanlimab, brentuximab vedotin
- Keywords
- NSCLC, cHL, HNSCC, TNBC, DLBCL, PTCL-NOS, Seattle Genetics
- Medical subject headings
- Carcinoma, Non-Small-Cell Lung, Stomach Neoplasms, Lymphoma, Large B-Cell, Diffuse, Lymphoma, T-Cell, Peripheral, Melanoma, Squamous Cell Carcinoma of Head and Neck, Urinary Bladder Neoplasms, Ovarian Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SEA-TGTDrug
Also called SGN-TGT
Given into the vein (IV; intravenously) on Day 1 of each 21-day cycle
sasanlimabDrug
Given via injection under the skin (subcutaneous) on Day 1 of each 21-day cycle
brentuximab vedotinDrug
Also called Adcetris
Given by IV on Day 1 of each 21-day cycle
| Study group | Role | What they receive |
|---|---|---|
| SEA-TGT Monotherapy (Parts A and B) | Experimental | SEA-TGT Receives: Drug: SEA-TGT |
| SEA-TGT + sasanlimab Combination Therapy (Part C) | Experimental | SEA-TGT + sasanlimab Receives: Drug: SEA-TGT; Drug: sasanlimab |
| SEA-TGT + brentuximab vedotin Combination Therapy (Part D) | Experimental | SEA-TGT + brentuximab vedotin Receives: Drug: SEA-TGT; Drug: brentuximab vedotin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of participants with adverse events (AEs)
An AE is any untoward medical occurrence in a subject or clinical investigational subject administered a medicinal product and which does not necessarily have a causal relationship with this treatment.
Measured: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Number of participants with laboratory abnormalities by grade
To be summarized using descriptive statistics
Measured: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Number of participants with a dose-limiting toxicity (DLT) at each dose level
To be summarized using descriptive statistics
Measured: Up to 21 days
Secondary outcomes (11)
Objective Response Rate (ORR)
Proportion of participants with complete response (CR) and partial response (PR) per the participant's specific tumor response criteria
Measured: Up to approximately 3 years
Complete response (CR) rate
Proportion of participants with CR per the participant's specific tumor response criteria
Measured: Up to approximately 3 years
Duration of objective response
Time from first response to the first documentation of disease progression or death due to any cause
Measured: Up to approximately 3 years
Duration of CR
Time from start of the first documentation of CR to the first documentation of confirmed tumor progression or to death due to any cause, whichever comes first
Measured: Up to approximately 3 years
Duration of progression-free survival
Time from first dose to the first documentation of disease progression or death due to any cause
Measured: Up to approximately 3 years
Duration of overall survival
Time from start of study treatment to the date of death due to any cause
Measured: Up to approximately 3 years
Area under the concentration-time curve (AUC)
To be summarized using descriptive statistics.
Measured: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Time to maximum concentration (tmax)
To be summarized using descriptive statistics.
Measured: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Maximum concentration (Cmax)
To be summarized using descriptive statistics.
Measured: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Trough concentration (Ctrough)
To be summarized using descriptive statistics.
Measured: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Number of participants with antidrug antibodies (ADA)
To be summarized using descriptive statistics.
Measured: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Feb 2020
- Study start29 May 2020
- Primary completion1 Dec 2023
- Study completion1 Dec 2023
Why it stopped: Study closed due to portfolio prioritization
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-small Cell Lung CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Enrolment
- 133 participants (actual)
Sponsor and investigators
- Lead sponsor
- Seagen Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Andres Forero-Torres, MD, Study director, Seagen Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04254107
- Sponsor's protocol ID
- SGNTGT-001
- Other IDs
- C5791001, 2019-004748-31, 2019
- Status last verified
- Feb 2025
- First submitted
- 31 Jan 2020
- Last updated
- 10 Feb 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Feb 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 1 Study of SEA-TGT (SGN-TGT) in Subjects With Advanced Malignancies
- ClinicalTrials.gov ID
- NCT04254107
- Acronym / sponsor ID
- SGNTGT-001
- Conditions
- Non-small Cell Lung Cancer, Gastric Carcinoma, Gastroesophageal Junction Carcinoma, Classical Hodgkin Lymphoma, Diffuse Large B-cell Lymphoma, Peripheral T-cell Lymphoma
- Keywords
- NSCLC, cHL, HNSCC, TNBC, DLBCL, PTCL-NOS, Seattle Genetics
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Study closed due to portfolio prioritization
- Enrolment
- 133 participants (actual)
- Lead sponsor
- Seagen Inc.Industry (pharma, biotech, devices)
- Study start
- 29 May 2020 (actual)
- Primary completion
- 1 Dec 2023 (actual)
- Study completion
- 1 Dec 2023 (actual)
- First posted
- 5 Feb 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This trial will look at a drug called SEA-TGT (also known as SGN-TGT) to find out whether it is safe for patients with solid tumors and lymphomas. It will study SEA-TGT to find out what its side effects are. A side effect is anything the drug does besides treating cancer. It will also study whether SEA-TGT works to treat solid tumors and lymphomas.
The study will have four parts. Part A of the study will find out how much SEA-TGT should be given to patients. Part B will use the dose found in Part A to find out how safe SEA-TGT is and if it works to treat solid tumors and lymphomas. Part C will study how well SEA-TGT with sasanlimab works to treat solid tumors. Part D will study how well SEA-TGT with brentuximab vedotin works to treat classical Hodgkin lymphoma (cHL).
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| SEA-TGT Monotherapy (Parts A and B) | Experimental | Drug: SEA-TGTSEA-TGT |
| SEA-TGT + sasanlimab Combination Therapy (Part C) | Experimental | Drug: SEA-TGT, Drug: sasanlimabSEA-TGT + sasanlimab |
| SEA-TGT + brentuximab vedotin Combination Therapy (Part D) | Experimental | Drug: SEA-TGT, Drug: brentuximab vedotinSEA-TGT + brentuximab vedotin |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| SEA-TGTAlso: SGN-TGTGiven into the vein (IV; intravenously) on Day 1 of each 21-day cycle | Drug | SEA-TGT + brentuximab vedotin Combination Therapy (Part D), SEA-TGT + sasanlimab Combination Therapy (Part C), SEA-TGT Monotherapy (Parts A and B) |
| sasanlimabGiven via injection under the skin (subcutaneous) on Day 1 of each 21-day cycle | Drug | SEA-TGT + sasanlimab Combination Therapy (Part C) |
| brentuximab vedotinAlso: AdcetrisGiven by IV on Day 1 of each 21-day cycle | Drug | SEA-TGT + brentuximab vedotin Combination Therapy (Part D) |
Primary outcome
Number of participants with adverse events (AEs)
Time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
An AE is any untoward medical occurrence in a subject or clinical investigational subject administered a medicinal product and which does not necessarily have a causal relationship with this treatment.
Number of participants with laboratory abnormalities by grade
Time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
To be summarized using descriptive statistics
Number of participants with a dose-limiting toxicity (DLT) at each dose level
Time frame: Up to 21 days
To be summarized using descriptive statistics
11 secondary outcomes
Objective Response Rate (ORR)
Time frame: Up to approximately 3 years
Complete response (CR) rate
Time frame: Up to approximately 3 years
Duration of objective response
Time frame: Up to approximately 3 years
Duration of CR
Time frame: Up to approximately 3 years
Duration of progression-free survival
Time frame: Up to approximately 3 years
Duration of overall survival
Time frame: Up to approximately 3 years
Area under the concentration-time curve (AUC)
Time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Time to maximum concentration (tmax)
Time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Maximum concentration (Cmax)
Time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Trough concentration (Ctrough)
Time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Number of participants with antidrug antibodies (ADA)
Time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years
Results and safety
The study was stopped early (reason given: Study closed due to portfolio prioritization). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Feb 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Andres Forero-Torres, MD study director
Seagen Inc.
36 sites in 6 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing SEA-TGT, sasanlimab and brentuximab vedotin in people with Non-small Cell Lung Cancer and Gastric Carcinoma, run by Seagen Inc. at 36 sites in 6 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 10 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 36 sites in United States, Spain, Canada, Italy, United Kingdom and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Study closed due to portfolio prioritization). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of participants with adverse events (AEs) (time frame: Through 45-52 days following last dose of SEA-TGT; up to approximately 3 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2025; AzTrials last refreshed its copy on 8 Nov 2026.