Seagen to Present New Clinical and Preclinical Data From Broad Portfolio of Targeted Cancer Therapeutics at the 2023 AACR Annual Meeting
Seagen Inc. (NASDAQ: SGEN) will present 17 abstracts at the upcoming AACR Annual Meeting from April 14-19, 2023, in Orlando, highlighting clinical and preclinical data. Key presentations include interim results from the innovaTV 207 Phase 2 trial of tisotumab vedotin for squamous cell carcinoma in head and neck cancer and initial Phase 1 data for SEA-TGT monotherapy in advanced malignancies. Seagen emphasizes its commitment to enhancing cancer treatment through innovative antibody-drug conjugate technologies.
- Presentation of 17 abstracts at AACR demonstrates active research and development.
- Interim results from the Phase 2 innovaTV 207 trial show progress for tisotumab vedotin in treating head and neck cancer.
- Initial Phase 1 data for SEA-TGT monotherapy may indicate potential in advanced malignancies.
- None.
- Interim results from Phase 2 innovaTV 207 trial of tisotumab vedotin in head and neck cancer to be presented -
- Initial Phase 1 dose-escalation data for SEA-TGT monotherapy in advanced malignancies to be disclosed -
- Preclinical data and discovery research underscore Seagen’s mission to innovate through next-generation ADC technologies -
“Seagen’s robust presence at AACR this year, highlighting progress across our diverse pipeline, underscores our commitment to improving and extending the lives of people living with cancer,” said
Highlights include an interim analysis from the innovaTV 207 Phase 2 study of tisotumab vedotin (TV) given every 2 weeks in patients with recurrent or metastatic squamous cell carcinoma of the head and neck who have progressed after prior platinum combination, immunotherapy, and targeted therapy, if eligible. TV, which is being developed in partnership with Genmab, is a tissue factor (TF)-directed antibody-drug conjugate (ADC). The innovaTV 207 study is currently ongoing and evaluating alternative dosing regimens of TV across multiple advanced solid tumors.
Other notable clinical data include initial results from a Phase 1 dose-escalation study of SEA-TGT monotherapy in patients with advanced malignancies. SEA-TGT is a novel investigational nonfucosylated human IgG1 antibody directed against TIGIT, an inhibitory immune checkpoint receptor that has emerged as a clinically relevant immuno-oncology target. SEA-TGT continues to be evaluated both as monotherapy and in combination with an anti-PD1 agent.
Additional preclinical data disclosures are planned, highlighting vedotin programs and novel ADC and tumor targeting technologies, including payloads with immune stimulatory properties.
Details of Seagen Presentations at AACR Annual Meeting 2023
Abstract Title |
Abstract # |
Presentation Time |
Lead Author |
ADCETRIS® (brentuximab vedotin) |
|||
CD30 is a marker of activated effector regulatory T cells in solid tumors providing clinical rationale for the combination of brentuximab vedotin and PD-1 inhibitors |
3253 |
Poster Presentation
Clinical Research Excluding Trials / Combination Immunotherapies 1
|
|
Exposure-response and age subgroup analyses to support body-weight (BW) dosing of brentuximab vedotin (BV) in newly diagnosed high-risk classical Hodgkin lymphoma (cHL) in children and young adults (aged 2-21 years [y]): A randomized Children’s |
6737 |
Poster Presentation
Clinical Research Excluding Trials / Preclinical Therapies and Clinical Observations in Pediatric Oncology
|
|
PADCEV® (enfortumab vedotin) |
|||
Enfortumab vedotin, a Nectin-4-directed antibody-drug conjugate, demonstrates compelling antitumor activity in non-muscle invasive bladder cancer models and accurately predicts minimal systemic exposure when administered by intravesical instillation in patients |
LB246 |
Poster Presentation
Tues.,
|
|
TIDVAK® (tisotumab vedotin) |
|||
Tisotumab vedotin (TV) in squamous cell carcinoma of head and neck (SCCHN): interim analysis from innovaTV 207 |
CT164 |
Poster Presentation
Phase II Clinical Trials 1
|
B. Cirauqui |
TUKYSA® (tucatinib) |
|||
Phase 3 study of tucatinib or placebo in combination with trastuzumab and pertuzumab as maintenance therapy for HER2+ metastatic breast cancer (HER2CLIMB-05, trial-in-progress) |
CT065 |
Poster Presentation
Phase II and Phase III Clinical Trials in Progress
|
|
Tucatinib does not alter oxaliplatin PK or associated renal function: An OCT2/MATE transport inhibition study |
5060 |
Poster Presentation
Experimental and Molecular Therapeutics - Theranostics and Radionuclides / Pharmacologic Approaches
Tues.,
|
|
Disitamab Vedotin |
|||
Disitamab vedotin, an investigational HER2-directed antibody-drug conjugate, shows potent antitumor activity as a monotherapy and in combination with tucatinib in preclinical cancer models |
560 |
Poster Presentation
Experimental and Molecular Therapeutics / Oncogenes and Tumor Suppressor Genes as Targets for Therapy 1
|
|
Early-Stage Programs |
|||
SGN-BB228, a CD228-directed costimulatory antibody anticalin bispecific provides potent and conditional 4-1BB costimulation to T cells in vivo and in an in vitro model of T-cell exhaustion
|
5676 |
Poster Presentation
Clinical Research Excluding Trials / Therapeutic Antibodies, Including Engineered Antibodies
Tues.,
|
|
SGN-B6A induces immunogenic cell death as an additional mechanism of action |
1522 |
Poster Presentation
Experimental and Molecular Therapeutics / Antibody-Drug Conjugates
|
|
Generation of an antibody-drug conjugate-optimized TLR7/8 agonist payload |
1542 |
Poster Presentation
Experimental and Molecular Therapeutics / Antibody-Drug Conjugates
|
|
Phase 1 dose-escalation study of SEA-TGT monotherapy in patients with advanced malignancies |
CT265 |
Poster Presentation
Phase I Clinical Trials 2
Tues.,
|
|
Using a clinical utility index (CUI) to determine the optimal biological dose of a nonfucosylated anti-TIGIT antibody: A proposed alternative to maximum tolerated dose (MTD) |
5668 |
Poster Presentation
Clinical Research Excluding Trials / Therapeutic Antibodies, Including Engineered Antibodies
Tues.,
|
G. Patilea-Vrana |
A preclinical model of acquired anti-PD-1 resistance is responsive to SEA-TGT, an effector-function enhanced anti-TIGIT monoclonal antibody |
6361 |
Poster Presentation
Immunology / Immune Checkpoints
|
|
A novel topoisomerase I inhibitor antibody-drug conjugate targeting CEACAM5 has potent antitumor activity in colorectal cancer models |
4890 |
Poster Presentation
Experimental and Molecular Therapeutics / Anticancer Approaches: Antibody-Drug Conjugates, Epigenetics, and Tumor Environment
Tues.,
|
|
|
|||
Oxidized anthracycline payloads induce antitumor immunogenic cell death and show linker-dependent tolerability when delivered as ADCs |
2013 |
Poster Presentation
Chemistry / Drug Delivery
|
|
Reversible chemical modification of antibodies: A complementary approach to tuning FcγR binding that maintains antitumor activity while mitigating peripheral immune activation |
2656 |
Poster Presentation
Experimental and Molecular Therapeutics / Antibody Technologies
|
|
MMAE drives immunomodulatory changes in a preclinical xenograft model that are distinct from other clinical-stage ADC payloads |
4892 |
Poster Presentation
Experimental and Molecular Therapeutics / Anticancer Approaches: Antibody-Drug Conjugates, Epigenetics, and Tumor Environment
Tues.,
|
|
About
Forward-Looking Statements
Certain statements made in this press release are forward-looking, such as those, among others, relating to the therapeutic potential of Seagen’s products and product candidates, including their potential efficacy, safety and therapeutic uses, as well as the company’s pipeline, technologies, collaborations and planned or ongoing clinical trials. Actual results or developments may differ materially from those projected or implied in these forward-looking statements. Factors that may cause such a difference include without limitation the difficulty and uncertainty of pharmaceutical product development, including the risks that the company may experience delays in its clinical trials or otherwise experience failures or setbacks in its clinical development programs due to lack of efficacy, adverse events or other factors, and that adverse regulatory actions may occur. More information about the risks and uncertainties faced by
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