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Neoplasms clinical trials

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NCT ID: NCT04857138 Completed - Solid Tumors Clinical Trials

A Study to Evaluate Safety, Pharmacokinetics and Anti-Tumor Activity of RO7300490, as Single Agent or in Combination With Atezolizumab in Participants With Advanced Solid Tumors

Start date: May 18, 2021
Phase: Phase 1
Study type: Interventional

A study to evaluate the safety, pharmacokinetics and anti-tumor activity of RO7300490 as a single agent or in combination with atezolizumab. The study will consist of 3 parts: [Part 1] Dose-Escalation of RO7300490 as a single agent; [Part 2] Dose-Escalation of RO7300490 in combination with atezolizumab and [Part 3] Dose-Expansion of RO7300490 in combination with atezolizumab in selected cancer types.

NCT ID: NCT04856774 Recruiting - Clinical trials for Advanced Solid Tumors

Trial of SHR-1701 Plus BP102 in Subjects With Selected Solid Tumors

Start date: June 1, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The main purpose of this study was to assess the safety, tolerability, and efficacy when combining SHR-1701 and BP102 in participants with certain cancers. This study was conducted in 2 phases, Phase Ib and Phase II.

NCT ID: NCT04856150 Recruiting - Clinical trials for Advanced Solid Tumors

A Study of Q-1802 in Patients With Advanced Solid Tumors

Start date: May 21, 2021
Phase: Phase 1
Study type: Interventional

Q-1802 is a bispecific antibody targeting both the tumor-specific antigen Claudin 18.2 and the immune checkpoint PD-L1. This is a multi-center, single-arm, open-label design to evaluate the safety and tolerance of Q-1802 in patients with advanced solid tumors, together with an assessment of pharmacokinetic characteristics and efficacy. The study consisted of two compartments: the dose-exploration stage and the dose-extension stage.

NCT ID: NCT04856020 Not yet recruiting - Pediatric Tumor Clinical Trials

Role of Gray Scale and Color Doppler Ultrasound in Diagnosis of Pediatric Neck Masses

Start date: April 2021
Phase:
Study type: Observational

Our aim is to assess the role of the gray scale and color Doppler ultrasound in diagnosis of the different pediatric neck masses .

NCT ID: NCT04855656 Recruiting - Clinical trials for Advanced Solid Tumor

Study of RP-6306 Alone or in Combination With RP-3500 or Debio 0123 in Patients With Advanced Solid Tumors

MYTHIC
Start date: April 30, 2021
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to assess the safety and tolerability of RP-6306 alone and in combination with RP-3500 or in combination with Debio 0123 in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) and assess preliminary anti-tumor activity.

NCT ID: NCT04855435 Recruiting - Clinical trials for Advanced Solid Tumor

Safety and Preliminary Efficacy of MBS8(1V270) in Cancer Patients With Advanced Solid Tumours

Start date: April 12, 2021
Phase: Phase 1
Study type: Interventional

The Phase I trial is planned to evaluate safety, tolerability, pharmacokinetics and preliminary efficacy of MBS8(1V270) in subjects with advanced solid tumours. The trial is designed to provide data for further clinical development of MBS8(1V270)

NCT ID: NCT04854681 Not yet recruiting - Clinical trials for Advanced Solid Tumors and Hematological Malignancies

Phase 1 Trial of the TQB2928 Injection in Patients With Advanced Cancers

Start date: August 1, 2021
Phase: Phase 1
Study type: Interventional

TQB2928 is a promising new molecular entity that mediates blockade of CD47 and SIRPα and enhances the phagocytosis of cancer cells by macrophages. In preclinical in vivo models, TQB2928 was active against a wide range of solid tumors and hematologic malignancies. This is the first-in-human phase 1 trial of TQB2928 in patients with advanced solid tumors and hematological malignancies.

NCT ID: NCT04854369 No longer available - Prostatic Neoplasms Clinical Trials

68Ga-PSMA-11 Patients With Newly Diagnosed and Recurrent Prostate Cancer (Firefly)

Firefly
Start date: n/a
Phase:
Study type: Expanded Access

This is a prospective, Phase 2, single-center, open-label study of 68Ga-PSMA-11 PET scans in patients with biochemically recurrent prostate cancer or those diagnosed and untreated with high risk or very high risk localized prostate cancer, or oligometastatic (defined as three or fewer metastatic lesions on conventional imaging) prostate cancer (using NCCN classification for localized disease). Approximately 300 patients are planned for enrollment in this study, divided into two cohorts. Cohort A will be 225 patients in the recurrent setting. Cohort B will be 75 patients in the up-front newly diagnosed setting. After a screening period (6-week window), eligible patients will undergo baseline assessments as per the Schedule of Study Activities. Patients will receive a single dose of 68Ga-PSMA-11 and undergo a PET/CT or PET/MRI imaging study.

NCT ID: NCT04853303 Not yet recruiting - Pain Clinical Trials

VR to Improve CINV, Sleep and Pain Among Children With Cancer in HK

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

Chemotherapy-induced nausea and vomiting, sleep quality and pain are the common symptoms experienced by children with cancer. These symptoms significantly devastate the children's quality of life. Hypnosis is found to be effective in managing chemotherapy-induced nausea and vomiting, sleep quality and pain in children with cancer. In addition, virtual reality is shown to promote the effectiveness of hypnosis in managing these symptoms. However, no study so far has examine it effectiveness in Hong Kong Chinese children with cancer. This study aims to investigate the effectiveness in the use a virtual reality device to improve chemotherapy-induced nausea and vomiting, sleep quality and pain among children with cancer in Hong Kong.

NCT ID: NCT04851119 Recruiting - Melanoma Clinical Trials

Tegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors

Start date: November 8, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial evaluates the highest safe dose, side effects, and possible benefits of tegavivint in treating patients with solid tumors that has come back (recurrent) or does not respond to treatment (refractory). Tegavivint interferes with the binding of beta-catenin to TBL1, which may help stop the growth of tumor cells by blocking the signals passed from one molecule to another inside a cell that tell a cell to grow.