Is NCT07509034 recruiting in Bethesda, MD?

Yes, NCT07509034 is currently recruiting participants at its Bethesda, MD location. This extensive-stage small cell lung cancer clinical trial is actively enrolling qualified participants.

Is participation in this Bethesda clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Extensive-Stage Small Cell Lung Cancer Clinical Trial in Bethesda, MD

Q: How do I join the extensive-stage small cell lung cancer clinical trial in Bethesda?

To join this clinical trial in Bethesda, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

About This Extensive-Stage Small Cell Lung Cancer Study in Bethesda

Background: Small cell lung cancer (SCLC) is the deadliest form of lung cancer. Extrapulmonary neuroendocrine cancer (EPNEC) is a similar type of cancer that develops anywhere other than the lungs. EPNEC is also deadly. B7-H3 is a protein often found in SCLC and EPNEC tumor cells. Researchers can modify a person s own T cells, or immune cells, to target B7-H3. When these modified T cells are returned to the body-a treatment called B7-H3 chimeric antigen receptor (CAR) T cell therapy-they may help kill cancer cells. Objective: To test B7-H3 CAR T cell therapy in people with SCLC or EPNEC. Eligibility: People aged 18 years and older with SCLC or EPNEC that either did not respond or returned after treatment. Design: Participants will be screened. They will have blood tests and tests of their heart function. They will have imaging scans. Participants will undergo apheresis: Blood will be taken from the body through a needle. The blood will pass through a machine that separates out the T cells. The remaining blood will be returned to the body through a different needle. The collected T cells will be altered to make them attack cells with B7-H3. Participants will be in the hospital for at least 15 days. They will receive chemotherapy drugs to prepare their body for the treatment. These drugs will be given through a tube attached to a needle inserted into a vein. The modified T cells will be infused through a vein. Participants will remain in the hospital until they are well enough to go home. Follow-up visits will continue for 15 years....

Sponsor: National Cancer Institute (NCI)

Who Can Participate

Inclusion Criteria

Age \>=18 years old.

Histologically confirmed small cell lung cancer (SCLC) or extrapulmonary neuroendocrine cancers (EP-NEC) that has recurred following or is refractory to first-line therapy. Note: small cell cancers of non-lung primary sites are also eligible.

Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0-2.

Pulse oximetry \>= 90% on room air.

Aspartate Transferase (AST) \< 3 X institutional upper limit of normal (ULN). Note: in case of liver metastases \<= 5 X ULN is acceptable.

Alanine Aminotransferase (ALT) \< 3 X institutional ULN. Note: in case of liver metastases \<= 5 X ULN is acceptable.

Total bilirubin \<=2 X institutional ULN.

Creatinine \<=1.5 X institutional ULN OR creatinine clearance (CrCl) \>= 50 mL/min/1.73m\^2 (calculated by the Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\] formula or calculated eGFR provided by a laboratory).

Absolute Neutrophil Count (ANC) \>= 750/mcL.

Platelet count \>= 75,000/mcL.

An absolute lymphocyte count (ALC) \>=300/mcL and CD3+ cell count \>=150/mcL.

Normal cardiac ejection fraction as defined by \>= 45% by echocardiogram (ECHO) at screening.

At least 1 measurable lesion by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 that has not been previously irradiated.

Recovered from acute toxic effects of all prior cancer therapy to Grade \<2 per Common Terminology Criteria for Adverse Events (CTCAE) v.6.0 at least one week before apheresis excluding the parameters for ANC and ALC mentioned above.

The following criteria must be met prior to apheresis:

Chemotherapy and biologic/targeted agents:

\>=14 days since the last dose of standard myelosuppressive chemotherapy.

\>= 7 days since the completion of biologic agent, targeted agent, or tyrosine kinase inhibitor therapy.

\>= 3 weeks or 5 half-lives (whichever is shorter) since prior therapy with a monoclonal antibody.

Radiotherapy:

\>= 1 week since the last radiotherapy session.

No washout period required for palliative radiation to non-target lesions.

\>= 3 weeks since hepatic radiation, chemoembolization, and/or radiofrequency ablation.

Steroids and immunosuppressive therapy:

Corticosteroids: \>= 2 weeks since the therapeutic doses (\> 0.5 mg/kg/day prednisone or equivalent). Note: Inhaled or topical steroids are not

Exclusion Criteria

Physiologic replacement doses (up to 5 mg/day prednisone equivalent) are allowed and can be adjusted based on participant's BMI if warranted.

\>= 2 weeks since the other immunosuppressive medication (e.g., calcineurin inhibitors, methotrexate, rapamycin, thalidomide, etc.).

Anti-PD-1 and any investigational therapies:

\>= 2 weeks since Anti-PD-1 monoclonal antibody therapy.

\>= 2 weeks or 5 half-lives of the investigational product (whichever is shorter) since any investigational treatment or clinical trial participation.

Other criteria:

72 hours since small molecule tyrosine kinase inhibitors (e.g., EGFR inhibitors), PARP inhibitors, or KRAS G12C inhibitors.

Individuals of childbearing potential (IOCBP) must agree to use highly effective contraception (hormonal, intrauterine device \[IUD\], abstinence, surgical sterilization) at the study entry and up to 12 months after the last dose of combined chemotherapy. Note: IOCBP is defined as any individual who has experienced menarche and who has not undergone successful surgical sterilization or who is not postmenopausal.

Individuals able to father a child must agree to use an effective method of contraception (barrier, surgical sterilization, abstinence) at the study entry and up to 7 months after the last dose of study drugs. We also will recommend individuals able to father a child with partners of childbearing potential ask partners to be on highly effective birth control (hormonal, IUD, surgical sterilization). Individuals able to father a child must not freeze or donate sperm within the same period.

Nursing participants must be willing to discontinue nursing from study treatment initiation through 6 months after the last dose of the study drug(s).

Ability of the participant to understand and the willingness to sign a written informed consent document. EXCLUSION CRITERIA:

History of anaphylactic reactions attributed to anti-B7-H3 antibodies or compounds of similar chemical or biologic composition to autologous B7-H3 CAR T cells, cyclophosphamide, fludarabine, or other agents used in this study.

Infection exposure with the human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV) as defined below:

Positive serology for HIV.

Active HBV infection as demonstrated by test for hepatitis B surface antigen (HBsAg).

Positive serology for HCV.

Prior gene therapy using an integrating vector (except for autologous B7-H3 CAR T cells retreatment).

History of any previous allogeneic hematopoietic stem cell transplant.

Presence of fungal, bacterial, viral, or other infection is permitted if responding to active treatment.

Central Nervous System (CNS) disorder such as cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, or autoimmune disease with CNS involvement that may impair the ability to evaluate neurotoxicity.

Pregnancy confirmed with beta-human chorionic gonadotropin (beta-HCG) serum or urine pregnancy test in IOCBP at screening.

Uncontrolled intercurrent illness or medical condition(s) evaluated by medical history, physical exam, electrocardiogram (ECG) or situations that would unacceptably increase risk for the participant or impair the ability to evaluate the endpoints of the study.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Bethesda?

Yes, this clinical trial (NCT07509034) has an active research site in Bethesda, MD that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Extensive-Stage Small Cell Lung Cancer Treatment Options in Bethesda, MD

If you're searching for extensive-stage small cell lung cancer treatment options in Bethesda, MD, this clinical trial (NCT07509034) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Bethesda research site is actively enrolling participants for this phase 1 clinical trial. You'll receive care from experienced extensive-stage small cell lung cancer specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all extensive-stage small cell lung cancer clinical trials near you to find additional studies recruiting in your area.

Extensive-Stage Small Cell Lung Cancer Clinical Trial in Bethesda, MD

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