SpokenWord Clinical Trials

Now enrolling: oncology clinical trials

We are currently enrolling participants 18 years of age or older for the following research studies. Qualified participants may receive study-related care. Compensation or reimbursement varies by study; please contact us for details. If you or someone you know may be eligible, please reach out for a confidential pre-screening.

Study 1 · Now enrolling

Extensive-Stage Small-Cell Lung Cancer (ES-SCLC)

Phase 3 Study of Sacituzumab Govitecan vs. Standard of Care topotecan in ES-SCLC

Purpose

To compare sacituzumab govitecan with standard-of-care topotecan in people with previously treated ES-SCLC.

Who can join?

You may qualify for this study if you:

  • Have ES-SCLC and radiological disease progression after one prior line of platinum-containing chemotherapy (at least 2 cycles), with or without anti-PD-1/PD-L1 therapy.
  • If previously treated with platinum-based therapy for LS-SCLC, that treatment may count as the prior line if radiological disease progression occurred 30–180 days after the last platinum dose.

Additional criteria apply.

Location
3465 Nazareth Road, Suite 102, Easton, PA 18045

Compensation or reimbursement
Please contact the study team for information about compensation or reimbursement.

Study 2 · Now enrolling

Advanced or Metastatic Non-Squamous NSCLC

Phase 2 Study of ABBV-400 plus Pembrolizumab or Standard-of-Care Treatment in Advanced or Metastatic NSCLC

Purpose

To evaluate ABBV-400 with pembrolizumab compared with standard-of-care pembrolizumab plus platinum/pemetrexed in previously untreated advanced or metastatic non-squamous NSCLC.

Who can join?

You may qualify for this study if you:

  • Have histologically documented, locally advanced or metastatic non-squamous NSCLC that is locally advanced or metastatic.
  • Have no prior systemic therapy for locally advanced or metastatic NSCLC. Certain prior adjuvant or neoadjuvant treatment may be allowed if completed at least 6 months before study treatment and there was no progression during treatment or within 6 months after completion.

Additional criteria apply.

Location
3465 Nazareth Road, Suite 102, Easton, PA 18045

Compensation or reimbursement
Please contact the study team for information about compensation or reimbursement.

Study 3 · Now enrolling

Limited-Stage Small-Cell Lung Cancer (LS-SCLC)

Phase 3 Study of Trilaciclib vs. Placebo During Concurrent Chemoradiation

Purpose

To evaluate whether trilaciclib can help prevent myelosuppression during concurrent chemoradiation for LS-SCLC.

Who can join?

You may qualify for this study if you:

  • Have confirmed LS-SCLC, stage I–III, without distant metastases.
  • Are eligible to receive concurrent chemoradiation.
  • Have not received cisplatin, carboplatin, etoposide, or trilaciclib for SCLC.

Additional criteria apply.

Location
3465 Nazareth Road, Suite 102, Easton, PA 18045

Compensation or reimbursement
Please contact the study team for information about compensation or reimbursement.

Study 4 · Now enrolling

FLT3-ITD-Positive Acute Myeloid Leukemia (AML) – Maintenance

Phase 2 Study of Quizartinib Maintenance Therapy in FLT3-ITD-Positive AML

Purpose

To compare the FDA-approved quizartinib maintenance dose (30 mg once daily) with a higher investigational dose (60 mg once daily) and further characterize safety and tolerability.

Who can join?

You may qualify for this study if you:

  • Are an adult with newly diagnosed FLT3-ITD-positive AML and are in first complete remission (CR1) after induction, with or without consolidation.
  • Have not received an allogeneic hematopoietic stem cell transplant (allo-HSCT).
  • Are a candidate for maintenance therapy and have adequate performance status and organ function.

Additional criteria apply.

Location
3465 Nazareth Road, Suite 102, Easton, PA 18045

Compensation or reimbursement
Please contact the study team for information about compensation or reimbursement.

Contact our research team

3465 Nazareth Road, Suite 102, Easton, PA 18045
(717) 819-9982 · Text us
[email protected]

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