Clinical trials

28

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Condition / disease
Location
Status: Recruiting

Feasibility and Acceptability of Collecting Sociodemographic Data in CCTG Trials

This study is being done to answer the following question: Are patients on a clinical trial willing to provide answers to questions about their social, economic, and environmental factors-sometimes called social determinants of health-which affect people's health experiences and access to care. These factors may include income, education, employment, housing, social supports, and experiences with discrimination or stress. Participation will help researchers better understand barriers to participating in clinical trials and access to health care.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Canadian Cancer Trials GroupUpdated: Aug 11, 2026Locations: 11
Eligibility criteria

Currently being screened and consented to a CCTG trial (prospective). [+1]

Participants already enrolled or expected to enroll in a CCTG trial that is also...

Status: Recruiting

Sonrotoclax Plus Zanubrutinib in Patients With Relapsed/Refractory Mantle Cell Lymphoma Planned for Standard of Care CAR-T Cell Therapy

The purpose of this study is to evaluate the effects of adding two oral medications (sonrotoclax plus zanubrutinib) to standard of care chimeric antigen receptor (CAR-T) cell therapy in participants with mantle cell lymphoma.

Participants needed: 40
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Aug 11, 2026Locations: 3
Eligibility criteria

Have histologically confirmed mantle cell lymphoma that is relapsed or refractor... [+18]

• Participants on active anticancer therapy for other advanced or metastatic mal... [+12]

Status: Recruiting

GCAR1, a Chimeric Antigen Receptor (CAR) T-CELL Therapy for Relapsed/Refractory GPNMB-Expressing Solid Tumours

Only enrolling in Canada. The purpose of this study is to identify the highest dose of GCAR1, a chimeric antigen receptor (CAR-T) cell therapy, that can be tolerated without causing very severe side effects, and to see what effects GCAR1 has on selected cancers

Participants needed: 30
Trial details
Phase: Phase 1Age: 15+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Aug 12, 2026Locations: 2
Eligibility criteria

Archival tumour specimen must be positive for GPNMB with high expression by immu... [+27]

Participants on active anticancer therapy for other advanced or metastatic malig... [+15]

Status: Recruiting

STRIDE (Durvalumab + Tremelimumab) With Lenvatinib vs STRIDE Alone in Unresectable Hepatocellular Carcinoma

The purpose of this study is to compare the effects on participants' and liver cancer by adding a drug that is used on its own to treat this disease to a combination of two other drugs which is also used to treat liver cancer, compared to the two-drug combination alone.

Participants needed: 140
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Aug 11, 2026Locations: 13
Eligibility criteria

Age ≥ 18 years. [+18]

Participants with a history of other malignancies, except: adequately treated no... [+20]

Status: Recruiting

Stereotactic Body Radiotherapy vs Conventional Palliative Radiotherapy for Painful Non-Spine Bone Metastases

This study is being done to answer the following question: Is Stereotactic Body Radiation Therapy or SBRT (a form of radiation therapy which can deliver high doses of radiation to the specific painful area of the body most affected by cancer, while keeping the radiation beams away from the healthy parts of the body that surround the cancer) better for pain relief than the standard treatment of conventional radiation therapy or CRT (a form of radiation therapy which delivers radiation to the painful area but can also negatively affect other parts of the body in the same area)

Participants needed: 230
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Aug 11, 2026Locations: 11
Eligibility criteria

Histologic confirmation of solid tumour. [+6]

Metastases of the hands, feet, cranium or spine (including sacrum) as the domina... [+6]

Status: Recruiting

STRatIfication of Vulvar SCC by HPV and p53 Status to Guide Excision

This study is being done to answer the following question: Are there types of early-stage vulvar cancer that require either less or more treatment than the usual approach?

Participants needed: 249
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Aug 11, 2026Locations: 12
Eligibility criteria

Histologically confirmed diagnosis of vulvar squamous cell carcinoma (VSCC) [+6]

Recurrent vulvar squamous cell carcinoma [+6]

Status: Recruiting

Paclitaxel and Ramucirumab +/- Zanidatamab in HER2 Postive Advanced Gastroesophageal Adenocarcinoma

This study is being done to answer the following question: Can the chance of gastroesophageal cancer growing or spreading be lowered by adding a drug called zanidatamab to the usual combination of drugs? We are doing this study because we want to find out if this approach is better or worse than the usual approach for this type of cancer. The usual approach is defined as care most people get for gastroesophageal cancer

Participants needed: 168
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Aug 11, 2026Locations: 18
Eligibility criteria

Participants must have histologically or pathologically confirmed gastroesophage... [+16]

Participants with a history of other malignancies except: adequately treated non... [+6]

Status: Recruiting

Adjuvant Therapy in POLE-Mutated and p53-Wildtype/NSMP Early Stage Endometrial Cancer RAINBO BLUE & TAPER

This protocol tests de-escalated adjuvant treatment in patients with POLE-mutated or p53wt/NSMP (p53 wildtype/no specific molecular profile) early-stage endometrial cancer (EC). Patients may be enrolled in one of two sub-studies * EN10.A/RAINBO BLUE: POLE-mutated EC * EN10.B/TAPER: p53 wildtype / NSMP EC

Participants needed: 393
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Aug 11, 2026Locations: 118
Eligibility criteria

Patients must have had surgery consisting of hysterectomy and bilateral salpingo... [+8]

Prior Neoadjuvant chemotherapy for current endometrial cancer diagnosis. [+5]

Status: Recruiting

Immunotherapy Platform Study in Platinum Resistant High Grade Serous Ovarian Cancer

This study is being done to answer the following question: What are the effects of a new drug or drugs on ovarian cancer? The pre-study screening may be done to test a sample of tissue for biomarkers to determine participation in the study.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 21, 2026Locations: 6
Eligibility criteria

This study will enroll women with platinum resistant high grade serous ovarian c... [+34]

Patients with a history of other malignancy may be eligible if curatively treate... [+18]

Status: Recruiting

Radiotherapy to Block Oligoprogression In Metastatic Non-Small-Cell Lung Cancer

This study is being done to answer the following question: Can the chance of lung cancer growing or spreading be lowered by adding targeted radiotherapy to the usual combination of drugs? This study is being done to find out if this approach is better or worse than the usual approach for lung cancer. The usual approach is defined as the care most people get for non-small cell lung cancer.

Participants needed: 320
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 75
Eligibility criteria

Metastatic disease (stage IV) detected on imaging and histologically and/or cyto... [+16]

Large-cell neuroendocrine carcinoma (LCNEC), pulmonary carcinoid tumour or mixed... [+8]

Status: Recruiting

Palliative Steroeotactic Body Radiotherapy vs Palliative Standard Radiotherapy in Patients With Advanced Head and Neck Cancer

This study is being done to answer the following question: Does stereotactic body radiation therapy (SBRT) provide better cancer control compared to standard radiation therapy (RT) for those with advanced head and neck cancer?

Participants needed: 196
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 9
Eligibility criteria

Histologically confirmed mucosal squamous cell carcinoma (SCC) of the head and n... [+9]

Patients with nasopharyngeal carcinoma. [+8]

Status: Recruiting

Docetaxel to Androgen Receptor Pathway Inhibitors in Patients With Metastatic Castration Sensitive Prostate Cancer and Suboptimal PSA Response

This study is being done to answer the following question: can the chance of prostate cancer growing or spreading be lowered by adding a drug to the usual combination of drugs? This study would like to find out if this approach is better or worse than the usual approach for prostate cancer. The usual approach for patients who are not in a study is hormone treatment with Androgen Deprivation Therapy (ADT) and Androgen-Receptor Pathway Inhibitor (ARPI).

Participants needed: 830
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 395
Eligibility criteria

Histologically/cytologically confirmed adenocarcinoma of the prostate or partici... [+18]

Confirmed PSA progression, defined by an increase in PSA of 25% above the nadir... [+13]

Status: Recruiting

Neoadjuvant Chemotherapy, Excision And Observation vs Chemoradiotherapy For Rectal Cancer

This study is being done to answer the following questions: Is the chance of rectal cancer responding the same if chemotherapy alone is given before limited surgery compared to chemotherapy and radiation therapy given together before limited surgery? If radiation therapy is not given, is quality of life better?

Participants needed: 250
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 113
Eligibility criteria

Histologically confirmed invasive, well-moderately differentiated rectal adenoca... [+13]

Pathologic high-risk factors on diagnostic biopsy: high histologic grade (poorly... [+12]

Status: Recruiting

Fixed Duration vs Continuous Anti-CD38 Antibody Therapy Among Transplant Ineligible Older Adults With Newly-Diagnosed Multiple Myeloma

Currently, daratumumab or isatuximab are given continuously (non-stop), along side lenalidomide, and dexamethasone as part of multiple myeloma treatment. are given continuously (non-stop). Recent observations suggest that stopping daratumumab or isatuximb after about a year and a half of treatment may work just as well as giving them continuously with lenalidomide and dexamethasone. Sometimes, bortezomib is also given. This study is being done to answer the question: is less daratumumab or isatuximab treatment as good as more?

Participants needed: 570
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 28
Eligibility criteria

Participants with newly diagnosed multiple myeloma that are transplant-ineligibl... [+9]

Known history of concurrent amyloid light chain amyloidosis, POEMS syndrome (pol... [+5]

Status: Recruiting

SPECT-CT Guided ELEctive Contralateral Neck Treatment for Patients With Lateralized Oropharyngeal Cancer

This study is being done to answer the following question: Is the chance of cancer spreading or returning the same if radiotherapy to the neck is guided, by using a special imaging study called lymph node mapping (lymphatic mapping) Single Photon Emission Computed Tomography (SPECT-CT), compared to the usual treatment when radiotherapy is given to both sides of the neck?

Participants needed: 510
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 38
Eligibility criteria

Patients with pathologically proven diagnosis of lateralized OPC (tonsil, tongue... [+16]

T1-T2 cancers isolated to the tonsil fossa (i.e. without any soft palate, tongue... [+9]

Status: Recruiting

Economic Analysis of Early vs Delayed Therapy in Newly Diagnosed Asymptomatic High-Risk Patients With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma:

Utilization data will be collected from all patients entered on the trial at Canadian centres from the time of registration until death, removal from study, or completion of 10 years of follow-up. Protocol-specified health care utilization will be collected within trial case report forms, and will include study visits, radiographic assessments, laboratory investigations, and treatment administration. Resource utilization data collection will be supplemented by a self-administered resource utilization form (Stanford SMRC) to document non-protocol specified utilization. This will include hospitalizations (including days in hospital), emergency room visits, and non-protocol specified ambulatory visits.

Participants needed: 247
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 6
Eligibility criteria

Patient must be eligible for the core CLC3/S1925 protocol. [+3]

Status: Recruiting

A Phase II Study of Durvalumab Treatment - Substudy A: In Patients Who Discontinued Prior Checkpoint Therapy Due to Immune Related Toxicity - Substudy B: For Continued Treatment (+/- Tremelimumab) of Patients Previously Enrolled to Completed CCTG Studies

I238A: The purpose of this study is to find out what effects being treated with durvalumab has on cancer. The researchers doing this study also want to evaluate if prednisone (a type of steroid), when given together with durvalumab, can reduce any side effects. I238B: The purpose of this study is to allow patients previously enrolled on a completed CCTG trial to continue treatment with durvalumab (+/- tremelimumab)

Participants needed: 60
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jul 14, 2026Locations: 11
Eligibility criteria

Patients must have histologically and/or cytologically confirmed solid tumour, t... [+29]

In general, patients with prior grade 4 non-hematological, non-endocrine immune-... [+17]

Status: Not yet recruiting

Canadian Initiative to Measure, Predict and Assess Cancer Treatment Outcomes in Patients Treated With Immuno-Oncotherapeutics

The researchers doing this study are interested in doing the following: * Biomarker research using fresh tumour tissue and normal blood cells, and if required, tumour tissue already collected. * Bio-banking for use in future research using the collected tumour tissue / blood .

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Canadian Cancer Trials GroupUpdated: Jun 30, 2026
Eligibility criteria

Willingness to submit a blood sample for buffy-coat and at least one tumour bios... [+2]

Status: Recruiting

Stereotactic Radiosurgery Compared With Hippocampal-Avoidant Whole Brain Radiotherapy (HA-WBRT) Plus Memantine for 5 or More Brain Metastases

Stereotactic radiosurgery (SRS) is a commonly used treatment for brain tumors. It is a one-day (or in some cases two day), out-patient procedure during which a high dose of radiation is delivered to small spots in the brain while excluding the surrounding normal brain. Whole brain radiation therapy with hippocampal avoidance (HA-WBRT) is when radiation therapy is given to the whole brain, while trying to decrease the amount of radiation that is delivered to the area of the hippocampus. The hippocampus is a brain structure that is important for memory. Memantine is a drug that is given to help relieve symptoms that can be caused by WBRT, including problems with memory and other mental symptoms. Health Canada, the regulatory body that oversees the use of drugs in Canada, has not approved the sale or use of memantine in combination with WBRT to treat this kind of cancer, although they have allowed its use in this study.

Participants needed: 206
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jun 9, 2026Locations: 86
Eligibility criteria

Patients must have 5 or more brain metastases as counted on a T1 contrast enhanc... [+14]

Pregnant or nursing women. [+15]

Status: Recruiting

Duration of Anti-PD-1 Therapy in Metastatic Melanoma

The purpose of this study is to compare the effects on patients with metastatic melanoma of taking a government approved and paid-for PD-1 inhibitor intermittently, with taking the same type of agent continuously. Researchers want to see if the two ways of giving this type of treatment work equally well in extending the life of patients with melanoma, or not.

Participants needed: 614
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Jun 9, 2026Locations: 30
Eligibility criteria

Histologically confirmed melanoma that is unresectable / metastatic (stage III o... [+9]

Patients not willing to stop anti-PD-1 therapy, if randomized to the intermitten... [+1]

Status: Recruiting

LND101 for Fecal Microbiota Transplantation in Combination With Immune Checkpoint Blockade in Advanced Melanoma

This study is being done to answer the following question: Can the chance of melanoma growing or spreading be lowered by receiving a treatment called LND101 for Fecal Microbiota Transplant (FMT) in addition to the usual immunotherapy treatment called Immune Checkpoint Blockade (ICB)? FMT treatment changes the bacteria in your gut called the microbiome.

Participants needed: 128
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: May 12, 2026Locations: 14
Eligibility criteria

Participants must have a confirmed histological diagnosis of cutaneous melanoma... [+17]

Participants with a prior or concurrent malignancy whose natural history or trea... [+17]

Status: Recruiting

Liquid-biopsy Informed Platform Trial to Evaluate CDK4/6-inhibitor Resistant ER+/HER2- Metastatic Breast Cancer

This study is being done to answer the following question: Can testing breast cancer for DNA abnormalities or "biomarkers" help predict which patients are most likely to be helped by certain treatments? The pre-study screening is being done to test a sample of blood (or tumour tissue) for biomarkers to see if patients can participate in the study

Participants needed: 484
Trial details
Phase: Phase 2Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: May 7, 2026Locations: 10
Eligibility criteria

Patients must have histologically and/or cytologically confirmed, advanced / met... [+33]

Patients with a history of other malignancies, including Myelodysplastic syndrom... [+19]

Status: Recruiting

Platinum and Taxane Chemo in Met Castration Resistant Prostate Cancer Patients With Alterations in DNA Damage Response Genes

The usual approach for most patients who are not in a study is treatment with docetaxel. This study is being done to answer the following question: Can the chance of prostate cancer growing or spreading be lowered by adding a drug to the usual approach? This study is being done to find out if this approach is better or worse than the usual approach for prostate cancer. The usual approach is defined as the care most people get for prostate cancer.

Participants needed: 236
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Apr 16, 2026Locations: 14
Eligibility criteria

Histologic diagnosis of adenocarcinoma of the prostate. The presence of neuroend... [+20]

Received prior platinum chemotherapy (i.e. carboplatin, cisplatin, oxaliplatin,... [+11]

Status: Recruiting

Androgen Suppression Combined With Nodal Irradiation and Dose Escalated Prostate Treatment

This study is being done to answer the following question: Is the strategy to give higher doses of radiotherapy treatment over a shorter period of time using special equipment and fewer treatments (also known as Stereotactic Body Radiation Therapy or SBRT) as effective as usual external radiation therapy given with a brachytherapy boost (which involves radiation sources inserted directly into the prostate)?

Participants needed: 710
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Apr 14, 2026Locations: 57
Eligibility criteria

Histologically confirmed adenocarcinoma of the prostate diagnosed within the las... [+24]

Prior pelvic radiotherapy [+7]

Status: Recruiting

Ibrutinib Combination Therapy in Transplant Ineligible Individuals With Newly Diagnosed Primary CNS Lymphoma

This study is being done to answer the following question: Can the addition of a new drug to the usual treatment lower the chance of primary central nervous system lymphoma growing or spreading? This study is being done to find out if this approach is better or worse than the usual approach for this type of cancer. The usual approach is defined as the care most people get for Primary Central Nervous System Lymphoma (PCNSL).

Participants needed: 30
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Canadian Cancer Trials GroupUpdated: Apr 14, 2026Locations: 8
Eligibility criteria

Patients must have histological or cytological evidence of primary central nervo... [+17]

Patients with secondary central nervous system non-Hodgkin lymphoma (NHL). [+27]