Clinical trials

64

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Condition / disease
Location
Status: Not yet recruiting

Phase I Trial of Pacritinib in Combination With Venetoclax and Azacitidine for the Treatment of Accelerated and Blast Phase Myeloproliferative Neoplasms

This phase I trial studies the side effects and best dose of pacritinib when given together with venetoclax and azacitidine in treating patients with accelerated and blast phase myeloproliferative neoplasms (MPN-AP/BP). Pacritinib and azacitidine may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein needed for cancer cell survival. Giving pacritinib together with venetoclax and azacitidine may be safe, tolerable, and/or effective in treating patients with MPN-AP/BP

Participants needed: 20
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2 [+9]

Diagnosis of de novo AML, acute promyelocytic leukemia, or accelerated or blast... [+13]

Status: Recruiting

Virtual Reality for Symptom Management in Patients Undergoing Hematopoietic Stem Cell Transplantation

This clinical trial compares the use of virtual reality to standard care for improving symptom management in patients undergoing hematopoietic stem cell transplantation (HSCT). Significant symptoms experienced by hospitalized HSCT patients include, but are not limited to, depression, tiredness, anxiety, drowsiness, lack of appetite, pain, and overall decreased quality of life and well-being. Virtual reality (VR) as an intervention can provide these patients with a much-needed escape from their reality and has proven results in clinical settings as a distraction therapy. VR technology targets the patient's auditory, visual, and physical contact/touch senses, and has been evidenced to improve depression, fatigue, anxiety, appetite, and pain. Virtual reality may improve symptom management in patients undergoing HSCT.

Participants needed: 28
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Adult patients (≥ 18 years old) admitted to Roswell Park on 5 North for planned... [+3]

Participants with known brain metastases should be excluded from this clinical t... [+6]

Status: Not yet recruiting

PK/PD of Vaping THC-containing Liquids vs. Smoked Cannabis

We will conduct a randomized, within-subjects clinical study to compare short-term pharmacokinetic (PK) and pharmacodynamic (PD) effects of Δ9-tetrahydrocannabinol (THC) vaping liquids vs. smoked cannabis containing 6 equivalent standard THC units (5 mg THC=1 Standard THC Unit (STU)) in healthy community members who are current users of both products. While smoking cannabis remains the most common mode of THC use among adults and youth, alternative modes of delivery, such as Electronic Vaping Products (EVPs), are becoming increasingly popular for the delivery of cannabinoids. Declining cannabis risk perceptions, increasing normalization of cannabis, greater legal access and availability to cannabis, ease of administration, and ability to conceal vaped THC use have likely contributed to increasing prevalence of use throughout the population across all age groups. Comparing vaping THC containing liquids with smoking cannabis can serve as an important benchmark for evaluating the delivery and effects of THC vaping products and, their relative safety

Participants needed: 40
Trial details
Phase: Phase 1Age: 21+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 30, 2026
Eligibility criteria

Age >= 21 years of age [+5]

• Illegal or non-prescription drug use within the past 90 days. As detected by N... [+9]

Status: Not yet recruiting

Home-Based Respiratory Muscle Training and Aerobic Exercise Programs to Improve Lung Health in Current and Former Cigarette Smokers

This clinical trial studies whether home-based respiratory muscle training (RMT) and aerobic exercise (AE) programs can be used to improve lung health in current and former cigarette smokers. Lung cancer, the leading cause of cancer death, is overwhelmingly caused by exposure to cigarette smoke. Research suggests that daily activity reduces lung cancer risk in current and former smokers. However, current and former smokers are generally not active and new approaches to improve lung health are needed. During the home-based RMT program, participants use a handheld device to complete breathing exercise sessions consisting of breathing in and out against adjustable resistance. During the home-based AE program, participants complete aerobic exercises using a stationary bike working at a moderate workload against adjustable resistance. The home-based RMT and AE programs may be effective ways to strengthen the breathing muscles, which may improve lung health in current and former cigarette smokers.

Participants needed: 200
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Age ≥ 50 years old [+5]

Any previous lung cancer diagnoses and or undergoing treatment for any cancer [+4]

Status: Recruiting

GB-5267 for the Treatment Platinum-Resistant Ovarian, Peritoneal, or Fallopian Tube Cancer

This phase 1 study evaluates the safety, efficacy, and biological activity of GB-5267 in patients with platinum-resistant ovarian cancer.

Participants needed: 18
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

At least 18 years of age [+22]

Recent significant bleeding, defined as a history of Grade ≥2 hemorrhage within... [+42]

Status: Recruiting

GT103 in Combination With Pembrolizumab for the Treatment of Advanced or Metastatic STK11 Mutant Non-Small Cell Lung Cancer

This phase II trial tests how well GT103 in combination with pembrolizumab works in treating patients with STK11 mutant non-small cell lung cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). GT103 is a monoclonal antibody that may interfere with the ability of cancer cells to grow and spread. GT103 targets the tumor cell-protein complement factor H found on some cancer cells and may provide specific anti-tumor activity that may help block the formation of growths that may become cancer. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving GT103 in combination with pembrolizumab may kill more cancer cells and improve outcomes in patients with advanced or metastatic STK11 mutant non-small cell lung cancer.

Participants needed: 28
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+15]

Receipt of anticancer chemotherapy within 4 weeks before the first administratio... [+19]

Status: Not yet recruiting

Photoimmunotherapy With ASP-1929 and Cemiplimab for the Treatment of Refractory, Inoperable, and Metastatic Stage IIIB-IV Non-small Cell Lung Cancer

This phase II trial tests how well photoimmunotherapy (PIT) with ASP-1929 in combination with cemiplimab works in treating patients with stage IIIB-IV non-small cell lung cancer (NSCLC) that has not responded to previous treatment (refractory), that is not suitable for surgery (inoperable), or that has spread from where it first started to other places in the body (metastatic). PIT is a treatment that combines drugs that become active when exposed to light, such as ASP-1929, with immunotherapy to target and kill tumor cells. ASP-1929 combines cetuximab with a light-sensitive component, sarotalocan. Cetuximab is in a class of medications called monoclonal antibodies. It binds to a protein called epidermal growth factor receptor (EGFR), which is found on some types of tumor cells. This may help keep tumor cells from growing. Sarotalocan is a fluorescent dye, infrared-activated fluorescent dye 700, that is light sensitive, and when activated by a special type of laser light, helps destroy or change tumor cells. Immunotherapy with monoclonal antibodies, such as cemiplimab, may help the body's immune system attack the tumor, and may interfere with the ability of tumor cells to grow and spread. Giving PIT with ASP-1929 in combination with cemiplimab may kill more tumor cells in patients with refractory, inoperable, or metastatic stage IIIB-IV NSCLC.

Participants needed: 27
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years of age [+15]

Has received an investigational agent within 30 days prior to initial treatment... [+29]

Status: Not yet recruiting

Psilocybin With Psychotherapy for Improving Chronic Pain in Cancer Patients Requiring Opioids

This phase II trial studies whether psilocybin with psychotherapy is safe and if it works for improving chronic pain in cancer patients who require opioids to manage their pain. Psilocybin is taken from the mushroom Psilocybe mexicana. Psilocybin acts on the brain to cause hallucinations (sights, sounds, smells, tastes, or touches that a person believes to be real but are not real). This may impact a patient's "total pain", a view that accounts for the psychological, spiritual, and social factors that contribute to their experience of pain. Psychotherapy uses methods such as discussion, listening, and counseling to help patients change the way they react to environmental triggers that may cause a negative reaction. Giving psilocybin with psychotherapy may be safe and helpful for improving chronic pain in cancer patients who require opioids to manage their pain.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Age ≥ 18 and ≤ 75 years old [+21]

Participants who are pregnant or breast-feeding [+29]

Status: Not yet recruiting

Evaluating the Delivery and Effects of THC Vaping Liquids in the Bloodstream

This clinical trial assesses differences in the delivery of THC to the bloodstream depending on whether nicotine vapes are used before or after THC. While there has been much recent publicity about vaping products and concern about their safety considering their increasing use for THC administration, the THC delivery profile associated with THC liquid vaping products in human subjects is currently unknown. Importantly, how the delivery to the bloodstream of THC vaping liquids compare to delivery from smoked cannabis, which is the most used method of cannabis delivery, will serve as an important benchmark for evaluating the delivery and effects of THC vaping products, and their relative safety.

Participants needed: 60
Trial details
Phase: Early Phase 1Age: 21+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Age ≥ 21 years of age; (self-reported on screening, verified at study visit). [+9]

Detection level 4-5 (> 300 ng/mL) on urinary THCA rapid test (NarcoCheck® THC Pr... [+16]

Status: Recruiting

Bipolar Androgen Therapy to Restore Sensitivity to Androgen Deprivation Therapy for Patients With Metastatic Castration Resistant Prostate Cancer

This phase I trial tests the change in androgen receptor sensitivity, side effects and effectiveness of bipolar androgen therapy, using testosterone, in patients with castration resistant prostate cancer that has spread to other places is the body (metastatic). Bipolar androgen therapy is the regulation of testosterone between castration levels (lower than what would be normally present) and supraphysiological levels (amounts greater than normally found in the body). This may suppress cancer cell growth, which reduces prostate-specific antigen (PSA) levels and may delay cancer progression.

Participants needed: 14
Trial details
Phase: Phase 1Age: 18+Biological sex: MaleType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years of age [+14]

Participants who have had chemotherapy or radiotherapy within 4 weeks (6 weeks f... [+11]

Status: Recruiting

Electrotherapy Stimulation Together With Life Coaching for the Support of Burnout Symptoms in Healthcare Workers

This clinical trial evaluates the effect of life coaching together with Cranial Electrotherapy Stimulation (CES) as an intervention to decrease self-reported symptoms of burnout, moral distress, resilience, and employee retention in oncology healthcare workers. Burnout and moral distress are occupational hazards for oncology healthcare workers. Emotional exhaustion, depersonalization, and lack of personal accomplishment at work are symptoms of burnout. Moral distress may be defined as knowing the right thing to do but being unable to do so based upon internal or external constraints. The device is attached to the earlobes that uses cranial electrotherapy stimulation (CES) at a microcurrent to alleviate symptoms of anxiety, insomnia, pain, and possibly depression. Life coaching is partnering with clients in a thought-provoking and creative process that inspires them to maximize their personal and professional potential and can increase resiliency skills such as boundary setting and prioritizing, increases in self-compassion and self-care, and potentially indirectly positively impact patient care. Undergoing the use of CES via the CES device, coupled with life coaching, may help alleviate burnout symptoms and moral distress in oncology healthcare workers.

Participants needed: 40
Trial details
Age: 21-75Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Age 21 ≤ and ≤ 75 years old [+11]

Subjects who self-report as pregnant or nursing. Pregnancy be verified with a ur... [+4]

Status: Recruiting

Genetically Engineered Cells (CD83 CAR T Cells) for the Treatment of Relapsed or Refractory Acute Myeloid Leukemia

This phase I trial tests the safety, side effects, and best dose of genetically engineered cells (CD83 chimeric antigen receptor \[CAR\] T cells) in treating patients with acute myeloid leukemia (AML) that has come back after a period of improvement (relapsed) or has not responded to previous treatment (refractory). CD83 is a protein that is found on AML blasts. Blasts are abnormal immature white blood cells that can multiply uncontrollably: filling up the bone marrow and preventing the production of other cells important for survival. CD83 CAR T cells represent a new cell therapy to eliminate AML blasts, while avoiding the risk for graft versus host disease (GVHD) after stem cell transplant to replace bone marrow or, tumor toxicity like myeloid aplasia where the body's own immune system causes damage to the bone marrow stem cells. Therefore, human CD83 CAR T cells are a promising cell-based approach to preventing two critical complications of stem-cell transplant - GVHD and relapse. Giving CD83 CAR T cells may be safe, tolerable, and/or effective in treating patients with relapsed or refractory AML.

Participants needed: 26
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years old. [+14]

Concomitant systemic glucocorticoid use at a dose equivalent to > 10 mg daily pr... [+13]

Status: Recruiting

Pegcetacoplan in Combination With Modified FOLFIRINOX for the Treatment of Metastatic Pancreatic Ductal Adenocarcinoma

This phase I/II trial tests the effect of pegcetacoplan in combination with oxaliplatin, irinotecan, leucovorin, and fluorouracil (mFOLFIRINOX) in treating patients with pancreatic ductal adenocarcinoma (PDAC) that has spread from where it first started (primary site) to other places in the body (metastatic). Pegcetacoplan works by targeting the immune complement process, a part of the immune system that defends against bacteria and may limit tumor progression and improve the immune system's response against tumor cells. Oxaliplatin is in a class of medications called platinum-containing antineoplastic agents. It damages the cell's deoxyribonucleic acid (DNA) and may kill tumor cells. Irinotecan is in a class of antineoplastic medications called topoisomerase I inhibitors. It blocks a certain enzyme needed for cell division and DNA repair and may kill tumor cells. Leucovorin is a drug used to lessen the toxic effects of substances that block the action of folic acid. Leucovorin is a form of folic acid. It is a type of chemoprotective agent and a type of chemosensitizing agent. Fluorouracil stops cells from making DNA and it may kill tumor cells. It is a type of antimetabolite. Giving pegcetacoplan in combination with mFOLFIRINOX may be safe, tolerable, and/or effecting in treating patients with metastatic PDAC. This trial also evaluates the effect of pegcetacoplan on the incidence of major thrombotic events and the resulting complications. Thrombosis is a common complication in patients with PDAC. Thrombosis occurs when blood clots block veins or arteries. Complications of thrombosis, such as stroke or heart attack, can be life-threatening. Giving pegcetacoplan may help prevent blood clots from forming and decrease the risk of major thrombotic events.

Participants needed: 35
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Histologically or cytologically confirmed metastatic PDAC [+16]

Previous chemotherapy for PDAC. Gemcitabine-based post- or pre-operative therapy... [+9]

Status: Recruiting

A Financial Intervention (Financial Compass) to Identify and Address Financial Hardship Among Head and Neck Cancer Patients, Financial Compass Trial

This clinical trial compares the effect a financial intervention, called Financial Compass, to usual care in identifying and addressing financial hardship in patients with head and neck cancer. Previous research has shown that head and neck cancer patients experiencing financial hardship have decreased overall and cancer specific survival. Using a financial intervention, Financial Compass, may be more effective than usual care in identifying and addressing financial hardship in patients with head and neck cancer.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

They have been diagnosed with head and neck cancer [+2]

Adults unable to complete the process of informed consent [+3]

Status: Recruiting

Fluorescence Image Guided Surgery Followed by Intraoperative Photodynamic Therapy for Improving Local Tumor Control in Patients With Locally Advanced or Recurrent Colorectal Cancer

\*As of June 2026- Phase I has been completed and we are now in Phase II. This phase I/II trial studies the side effects and how well fluorescence image guided surgery followed by intraoperative photodynamic therapy for improving local tumor control in patients with colorectal cancer that has spread to nearby tissue or lymph nodes (locally advanced) or that has come back after a period of improvement (recurrent). Fluorescence image guided surgery uses a drug named aminolevulinic acid hydrochloride. Aminolevulinic acid hydrochloride is a photosensitizing agent, meaning that is activated by light and, is converted to another drug in cancer cells more than in normal cells. The converted drug emits fluorescence red light when activated with low power blue light. It is used to assist the surgeon to see cancer cells and small cancerous tissue that may have been missed during routine surgery. In addition to emitting fluorescence light, the converted drug in the cancer cells and tissue can be activated with red laser light to kill cancer cells. This procedure is called photodynamic therapy (PDT). Performing fluorescence image guided surgery followed by intraoperative photodynamic therapy after the surgical removal of the colorectal tumor before the surgical site will be closed may be effective and improve outcomes in patients with locally advanced or recurrent colorectal cancer.

Participants needed: 21
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years of age [+5]

Pregnant or nursing female participants [+7]

Status: Recruiting

Pilot Study of Line-Field Confocal Optical Coherence Tomography for Detection of Mohs Micrographic Surgery Margins of Basal Cell Carcinomas

To assess the feasibility and provide information on the utility of noninvasive line field confocal optical coherence tomography (LC-OCT) for the presurgical assessment of Mohs micrographic surgery sites in patients undergoing removal of cutaneous basal cell carcinomas (BCC).

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years [+3]

Known or reported allergy to mineral oil, the optical agent used during imaging. [+3]

Status: Recruiting

Influence of Authorized Smokeless Tobacco Product Modified Risk Claims I: Consumer Product Demand

To explore consumer responses to the announcement and implementation of new modified risk claims for Copenhagen and General Snus (brands of smokeless tobacco (ST) products) using a series of complementary and innovative research activities and methods.

Participants needed: 160
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Residing in one of the 8 counties of Western New York (Erie, Niagara, Cattaraugu... [+5]

Plan to quit smoking in the next 30 days. [+4]

Status: Recruiting

Pembrolizumab Combined With Bevacizumab With or Without Agonist Anti-CD40 CDX-1140 for the Treatment of Patients With Recurrent Ovarian Cancer

This phase II trial tests whether pembrolizumab combined with bevacizumab with or without agonist anti-CD40 CDX-1140 works to shrink tumors in patients with ovarian cancer that has come back (recurrent). Anti-CD40 CDX-1140 works by stimulating certain immune cells within the tumor and, when combined with other immunotherapy treatments, may increase antitumor antibody production. Immunotherapy with monoclonal antibodies, such as pembrolizumab and bevacizumab, may help the body's immune system, and may interfere with the ability of tumor cells to grow and spread. Giving pembrolizumab and bevacizumab with anti-CD40 CDX-1140 may decrease symptoms, prolong survival, and improve quality of life in patients with ovarian cancer.

Participants needed: 80
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: Jun 1, 2026Locations: 2
Eligibility criteria

Age >= 18 years of age. [+22]

Primary platinum-refractory patients are excluded [+34]

Status: Recruiting

New York Better Breathing Study

This clinical trial evaluates the effects of whether breathing exercises at home can reduce symptoms and help stage I-III lung cancer survivors stay active. Over 70% of lung cancer survivors have trouble breathing, feel tired, and have lower levels of fitness. This is often because their breathing muscles are weaker after surgery. Many survivors find it hard to exercise, which affects their quality of life and overall survival. A training program to strengthen these muscles might reduce breathing problems, lower fatigue, and improve quality of life. Staying active could also help boost the immune system to fight cancer. Respiratory muscle training (RMT) involves a series of breathing and other exercises that are performed to improve the function of the respiratory muscles through resistance and endurance training. Participating in a home-based RMT intervention may reduce symptoms from cancer or treatment in lung cancer survivors.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: May 28, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years of age. [+6]

Participant has in situ (stage 0) or metastatic (stage IV) disease at study entr... [+4]

Status: Recruiting

Temozolomide and Survivin Long Peptide Vaccine (SurVaxM) for the Treatment of Patients With Progressing Metastatic Neuroendocrine Carcinomas

This phase IIa trial compares the safety and effect of temozolomide combined with survivin long peptide vaccine (SurVaxM) to temozolomide alone in patients with neuroendocrine tumors (NET) that has spread from where it first started (primary site) to other places in the body (metastatic) and is growing, spreading or getting worse (progressing). Temozolomide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid and may kill tumor cells and slow down or stop tumor growth. Survivin, a protein, is expressed in 50% of patients that have neuroendocrine tumors and, is associated with poor outcomes. SVN53-67/M57-KLH peptide vaccine (SurVaxM) is a vaccine that has been shown to produce an immune system response against cancer cells that express a survivin and may block the growth of new tumor cells. Giving temozolomide with SurVaxM may kill more tumor cells in patients with progressing metastatic neuroendocrine tumors.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: May 28, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years of age [+15]

Patients who have received temozolomide in the advanced disease setting either a... [+12]

Status: Recruiting

Home-based Respiratory Muscle Training for Minimizing Side Effects in Patients Undergoing Treatment for Cancer

This clinical trial evaluates whether home-based respiratory muscle training is useful for minimizing side effects in patients undergoing treatment for cancer. Over-activation of the nervous system during breast cancer treatment can result in heart- and lung-related side effects which have the potential to reduce a patient's quality of life. Aerobic exercise can help prevent the development of these side effects. However, engaging in regular aerobic exercise may be difficult for breast cancer patients who are actively undergoing treatment. Respiratory muscle training (RMT) involves a series of breathing and other exercises that are performed to improve the function of the respiratory muscles through resistance and endurance training. Home-based RMT may represent a more feasible approach for reducing side effects in patients undergoing treatment for breast cancer.

Participants needed: 130
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: May 29, 2026Locations: 1
Eligibility criteria

Documented breast cancer and scheduled to receive adjuvant or neoadjuvant chemot... [+4]

Presence of oral mucosal disease including oral mucositis, or oral candidiasis d... [+2]

Status: Recruiting

Understanding Tobacco and Cannabis Co-Use Practices: Initiation, Escalation, and Maintenance

This study evaluates histories among cannabis and tobacco co-users of their initiation, escalation, and maintenance of the co-use behavior.

Participants needed: 40
Trial details
Age: 18-30Biological sex: AllType: ObservationalSponsor: Roswell Park Cancer InstituteUpdated: May 22, 2026Locations: 1
Eligibility criteria

* Adults aged 18 to 30 years old. [+5]

* Unwilling or unable to follow protocol requirements. [+2]

Status: Not yet recruiting

Transperineal Micro-ultrasound for the Detection of Prostate Cancer During Biopsy

This clinical trial studies whether transperineal micro-ultrasound can be used to detect prostate cancer during biopsy. Transrectal ultrasound is often used during prostate biopsy. Transrectal ultrasound imaging is a procedure in which a probe that sends out high-energy sound waves is inserted into the rectum. The sound waves are bounced off internal tissues or organs and make echoes. The echoes form a picture of body tissue called a sonogram. Transrectal ultrasound is used to look for abnormalities in the rectum and nearby structures, including the prostate. The images are used to guide the prostate biopsy. Transperineal micro-ultrasound is completed by placing a probe over the skin between the scrotum and anus (perineum). It is a high-resolution ultrasound at 29 megahertz (MHz) (compared to traditional ultrasound at 6-9 MHz). This higher frequency allows for an improved spatial resolution. This improved spatial resolution is approximately the diameter of a prostatic duct, and therefore, may be able to visualize slight changes in the structure of prostatic ducts that are not possible with standard transrectal ultrasound. Transperineal micro-ultrasound may be more effective in detecting prostate cancer during biopsy.

Participants needed: 138
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: May 22, 2026Locations: 1
Eligibility criteria

Men aged ≥ 18 years [+2]

Any condition which in the investigator's opinion deems the participant an unsui...

Status: Recruiting

Influence of Authorized Smokeless Tobacco Product Modified Risk Claims II: Laboratory Assessment of Sensory and Subjective Effects

This study seeks to measure the effects of smokeless tobacco product risk messages on sensory experiences and future intentions to use.

Participants needed: 50
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: May 22, 2026Locations: 1
Eligibility criteria

Age ≥ 21 years of age [+8]

Age ≥ 21 years of age [+8]

Status: Recruiting

Nemtabrutinib and Pembrolizumab for the Treatment of Richter Transformation, Diffuse Large B-cell Lymphoma Subtype

This phase II trial tests how well nemtabrutinib in combination with pembrolizumab works in treating patients with Richter transformation, diffuse large B-cell lymphoma subtype (RT-DLBCL). Nemtabrutinib is in a class of medications called kinase inhibitors. It blocks a protein called BTK, which is present on B-cells (a type of white blood cell) in cancers such as Richter transformation at abnormal levels. This may help keep cancer cells from growing and spreading. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of cancer cells to grow and spread. Giving nemtabrutinib in combination with pembrolizumab may kill more cancer cells in patients with RT-DLBCL.

Participants needed: 32
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: May 20, 2026Locations: 1
Eligibility criteria

Patients with biopsy-proven Richter transformation, diffuse large B-cell lymphom... [+24]

Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PDL2 agent or... [+25]