Purpose

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 three 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.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

(Parts A and B) - Histologically- or cytologically-confirmed advanced or metastatic malignancy, defined as: - One of the following disease indications: - Unresectable locally-advanced or metastatic 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: - Classical Hodgkin lymphoma (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 (≤24 months from screening). If archived tissue is not available, a fresh screening 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 - Participants with a local histologically-confirmed advanced NSCLC TPS ≥50% and 1-49%, cutaneous melanoma (excluding acral or mucosal varieties), and HNSCC meeting at least 1 of the following criteria: - NSCLC: histological or cytological confirmed metastatic disease. Participants must have received no prior systemic regimen in the metastatic setting and no prior anti-PD-1 therapy allowed. - HNSCC: histological or cytological confirmed metastatic disease. Participants must have received no prior systemic therapy in the metastatic setting and no prior exposure to anti-PD-L1 therapy. - Cutaneous Melanoma: histological or cytological confirmed metastatic disease. Particpants must not have received anti-PD-1 targeted therapy. - Measurable disease by CT or magnetic resonance imaging (MRI) as defined by RECIST V1.1 - Participants must provide archived tumor tissue, if available, from the most recent biopsy (≤24 months from screening). If archived tissue is not available, a fresh screening tumor biopsy will be requested 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, 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 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. - 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, antibody-drug conjugates, 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

Study Design

Phase
Phase 1
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Sequential Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Monotherapy (Parts A and B)
  • Drug: SEA-TGT
    Given into the vein (IV; intravenously) on Day 1 of each 21-day cycle
    Other names:
    • SGN-TGT
Experimental
Combination Therapy (Part C)
  • Drug: SEA-TGT
    Given into the vein (IV; intravenously) on Day 1 of each 21-day cycle
    Other names:
    • SGN-TGT
  • Drug: sasanlimab
    Given via injection under the skin (subcutaneous) on Day 1 of each 21-day cycle

Recruiting Locations

University of Alabama at Birmingham
Birmingham, Alabama 35249
Contact:
Jenny King
jpking@uabmc.edu

More Details

Status
Recruiting
Sponsor
Seagen Inc.

Study Contact

Seagen Trial Information Support
866-333-7436
clinicaltrials@seagen.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.