Search Clinical Trials
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Building Resiliency Among Caregivers of Curvivors and Metavivors
Massachusetts General Hospital
Stress
Cancer Diagnosis
Distress, Emotional
The main purpose of this research study is to assess the feasibility and participants'
satisfaction of the Stress Management and Resiliency - Relaxation Response Resiliency
Program (SMART-3RP) and compare this treatment with SMART-3RP versus referral to a
group-based, online support group to see wh1 expand
The main purpose of this research study is to assess the feasibility and participants' satisfaction of the Stress Management and Resiliency - Relaxation Response Resiliency Program (SMART-3RP) and compare this treatment with SMART-3RP versus referral to a group-based, online support group to see which is better for improving resilience and decreasing distress of participants with cancer and their caregivers. The name of the study intervention involved in this study is: Smart-3RP (virtual, mind-body group treatment program). Type: Interventional Start Date: Jun 2023 |
Study of Iadademstat and Gilteritinib in Patients With R/R AML With FMS-like Tyrosine Kinase Mutati1
Oryzon Genomics S.A.
Acute Myeloid Leukemia, in Relapse
Acute Myeloid Leukemia Refractory
Iadademstat is being studied as a treatment for subjects with Relapsed or Refractory
Acute Myeloid Leukemia (R/R AML) with FMS-like tyrosine kinase mutation (FLT3 mut+).
During the trial, iadademstat will be given in combination with gilteritinib, a drug that
is already approved to treat patients w1 expand
Iadademstat is being studied as a treatment for subjects with Relapsed or Refractory Acute Myeloid Leukemia (R/R AML) with FMS-like tyrosine kinase mutation (FLT3 mut+). During the trial, iadademstat will be given in combination with gilteritinib, a drug that is already approved to treat patients with FLT3-mutated R/R AML. Type: Interventional Start Date: Nov 2022 |
A Phase I/II Study of DYP688 in Patients With Metastatic Uveal Melanoma and Other GNAQ/11 Mutant Me1
Novartis Pharmaceuticals
Metastatic Uveal Melanoma
This is a FIH, phase I/II, open label, multi-center study of DYP688 as a single agent.
The purpose of this study is to characterize the safety, tolerability, and anti-tumor
activity of DYP688 as a single agent in patients with metastatic uveal melanoma (MUM) and
other melanomas harboring GNAQ/11 mu1 expand
This is a FIH, phase I/II, open label, multi-center study of DYP688 as a single agent. The purpose of this study is to characterize the safety, tolerability, and anti-tumor activity of DYP688 as a single agent in patients with metastatic uveal melanoma (MUM) and other melanomas harboring GNAQ/11 mutations. Type: Interventional Start Date: Jul 2022 |
Study of Tirabrutinib (ONO-4059) in Patients With Primary Central Nervous System Lymphoma (PROSPECT1
Ono Pharmaceutical Co. Ltd
Refractory Primary Central Nervous System Lymphoma
Primary CNS Lymphoma
This study will evaluate the efficacy, safety, and pharmacokinetics of tirabrutinib
monotherapy in patients with relapsed or refractory PCNSL (Part A), and tirabrutinib in
combination with one of two different high dose methotrexate based regimens
(methotrexate/ temozolomide/rituximab or rituximab/1 expand
This study will evaluate the efficacy, safety, and pharmacokinetics of tirabrutinib monotherapy in patients with relapsed or refractory PCNSL (Part A), and tirabrutinib in combination with one of two different high dose methotrexate based regimens (methotrexate/ temozolomide/rituximab or rituximab/methotrexate/procarbazine/ vincristine) as first line therapy in patients with newly diagnosed, treatment naïve PCNSL (Part B) Type: Interventional Start Date: Dec 2021 |
Estrogen Administration for the Treatment of NASH in Postmenopausal Women
Massachusetts General Hospital
NASH - Nonalcoholic Steatohepatitis
Non-alcoholic fatty liver disease (NAFLD) is a growing epidemic in the United States.
Despite this, the treatment options remain limited. Preclinical and preliminary clinical
data suggest that estrogen deficiency plays an important role in the pathology of
steatosis, inflammation and fibrosis in no1 expand
Non-alcoholic fatty liver disease (NAFLD) is a growing epidemic in the United States. Despite this, the treatment options remain limited. Preclinical and preliminary clinical data suggest that estrogen deficiency plays an important role in the pathology of steatosis, inflammation and fibrosis in non-alcoholic steatohepatitis (NASH), the progressive form of NAFLD. Post-menopausal women are a growing population with particularly high risk of NASH due to their lack of estrogen. This study will examine the effect of estradiol on hepatic fibrosis and fat in post-menopausal women with NASH. Type: Interventional Start Date: Dec 2021 |
Prolonged Pulsatile Kisspeptin Administration in Hypogonadotropic Hypogonadism
Stephanie B. Seminara, MD
Hypogonadotropic Hypogonadism
The goal of this study is to develop novel treatments for patients with a condition
called hypogonadotropic hypogonadism (HH) through the use of exogenous kisspeptin. expand
The goal of this study is to develop novel treatments for patients with a condition called hypogonadotropic hypogonadism (HH) through the use of exogenous kisspeptin. Type: Interventional Start Date: Jan 2021 |
Improving Attentional and Cognitive Control in the Psychological Treatment of Intrusive Thoughts
Massachusetts General Hospital
Obsessive-Compulsive Disorder
Generalized Anxiety Disorder
Major Depressive Disorder
The investigators are conducting this study to learn more about the cognitive and
attentional processes among individuals with three types of repetitive negative thinking
(RNT): mental rituals (as seen in obsessive compulsive disorder, OCD), worries (as seen
in generalized anxiety disorder, GAD), a1 expand
The investigators are conducting this study to learn more about the cognitive and attentional processes among individuals with three types of repetitive negative thinking (RNT): mental rituals (as seen in obsessive compulsive disorder, OCD), worries (as seen in generalized anxiety disorder, GAD), and ruminations (as seen in major depressive disorder, MDD). Specifically, the investigators are studying whether psychological treatment can help people with RNT who have trouble stopping unwanted thoughts and shifting their attention. Type: Interventional Start Date: Apr 2021 |
Study to Evaluate Safety, Tolerability, and Optimal Dose of Candidate GBM Vaccine VBI-1901 in Recur1
VBI Vaccines Inc.
Glioblastoma Multiforme
The purpose of this study is to assess the safety and tolerability of VBI-1901 in
subjects with recurrent malignant gliomas (glioblastoma, or GBM). expand
The purpose of this study is to assess the safety and tolerability of VBI-1901 in subjects with recurrent malignant gliomas (glioblastoma, or GBM). Type: Interventional Start Date: Dec 2017 |
Permissive Hypotension After Cardiac Surgery
Massachusetts General Hospital
Surgery
The objective of this pilot randomized controlled trial is to demonstrate the feasibility
of implementing a pragmatic clinical trial randomizing patients to permissive hypotension
versus usual care and to determine the impact of permissive hypotension on vasopressor
exposure, ICU length of stay, ma1 expand
The objective of this pilot randomized controlled trial is to demonstrate the feasibility of implementing a pragmatic clinical trial randomizing patients to permissive hypotension versus usual care and to determine the impact of permissive hypotension on vasopressor exposure, ICU length of stay, markers of end organ perfusion, and clinically relevant patient outcomes. The data collected from this pilot study will be used as preliminary data for study design and grant applications for a larger multicenter randomized controlled trial. Type: Interventional Start Date: Apr 2024 |
FOG-001 in Locally Advanced or Metastatic Solid Tumors
Fog Pharmaceuticals, Inc.
Cancer
Colorectal Cancer
Solid Tumor
Locally Advanced Solid Tumor
Metastatic Cancer
The goal of this clinical trial is to determine if FOG-001 is safe and effective in
participants with locally advanced or metastatic cancer. expand
The goal of this clinical trial is to determine if FOG-001 is safe and effective in participants with locally advanced or metastatic cancer. Type: Interventional Start Date: May 2023 |
Delayed Tolerance Through Mixed Chimerism
Massachusetts General Hospital
Kidney Failure
Kidney Transplant; Complications
Chimera
This study will examine the safety and effectiveness of a bone marrow transplant after
kidney transplant (from either a living or deceased donor). An investigational medication
and other treatments will be given prior to and after the transplant to help protect the
transplanted kidney from being at1 expand
This study will examine the safety and effectiveness of a bone marrow transplant after kidney transplant (from either a living or deceased donor). An investigational medication and other treatments will be given prior to and after the transplant to help protect the transplanted kidney from being attacked by the body's immune system Type: Interventional Start Date: Oct 2023 |
Study of MRTX1133 in Patients With Advanced Solid Tumors Harboring a KRAS G12D Mutation
Mirati Therapeutics Inc.
Solid Tumor
Advanced Solid Tumor
Non-small Cell Lung Cancer
Colo-rectal Cancer
Pancreatic Adenocarcinoma
A Phase 1/2 study of MRTX1133 in solid tumors harboring a KRAS G12D mutation. expand
A Phase 1/2 study of MRTX1133 in solid tumors harboring a KRAS G12D mutation. Type: Interventional Start Date: Mar 2023 |
A Study to Evaluate the Safety and Tolerability of TOS-358 in Adults With Select Solid Tumors
Totus Medicines
Colorectal Cancer
Gastric Cancer
HER2-negative Breast Cancer
Non-small Cell Lung Cancer
Squamous Cell Carcinoma of Head and Neck
The goal of this clinical trial is to evaluate the safety of TOS-358 in adults with
select solid tumors who meet study enrollment criteria. The main questions it aims to
answer are:
1. what is the maximum tolerated dose and recommended dose for phase 2?
2. how safe and tolerable is TOS-358 at1 expand
The goal of this clinical trial is to evaluate the safety of TOS-358 in adults with select solid tumors who meet study enrollment criteria. The main questions it aims to answer are: 1. what is the maximum tolerated dose and recommended dose for phase 2? 2. how safe and tolerable is TOS-358 at different dose levels when taken orally once or twice per day? Type: Interventional Start Date: Feb 2023 |
Neuroactive Steroid to Treat Depressed Mood: A Trial for People With HIV
Massachusetts General Hospital
Major Depressive Disorder
Anxiety Depression
HIV
This study will determine the effects of pregnenolone on brain function, inflammation and
depressive symptoms in people with HIV who have depression. Participants in this study
will receive a pill of either pregnenolone or placebo, and can stay on their current
antidepression medications. Brain ima1 expand
This study will determine the effects of pregnenolone on brain function, inflammation and depressive symptoms in people with HIV who have depression. Participants in this study will receive a pill of either pregnenolone or placebo, and can stay on their current antidepression medications. Brain imaging and behavioral assessments will be performed during the study. Type: Interventional Start Date: Mar 2023 |
Computational Neuroscience of Language Processing in the Human Brain
Massachusetts General Hospital
Language
Epilepsy
Language is a signature human cognitive skill, but the precise computations that support
language understanding remain unknown. This study aims to combine high-quality human
neural data obtained through intracranial recordings with advances in computational
modeling of human cognition to shed light1 expand
Language is a signature human cognitive skill, but the precise computations that support language understanding remain unknown. This study aims to combine high-quality human neural data obtained through intracranial recordings with advances in computational modeling of human cognition to shed light on the construction and understanding of speech. Type: Interventional Start Date: Apr 2021 |
FOLFIRINOX + 9-Ing-41 + Losartan In Pancreatic Cancer
Colin D. Weekes, M.D., PhD
Pancreatic Adenocarcinoma
Pancreatic Adenocarcinoma Metastatic
The purpose of this study is to find out if an experimental drug will prevent metastatic
pancreatic adenocarcinoma from becoming resistant to standard treatment for the disease.
The names of the study drugs involved in this study are:
- 9-ING-41
- Losartan
- Ferumoxytol
- FOLFIRINO1 expand
The purpose of this study is to find out if an experimental drug will prevent metastatic pancreatic adenocarcinoma from becoming resistant to standard treatment for the disease. The names of the study drugs involved in this study are: - 9-ING-41 - Losartan - Ferumoxytol - FOLFIRINOX (made up of 4 different drugs): - 5-Fluorouracil (5-FU) - Oxaliplatin - Irinotecan - Leucovorin Type: Interventional Start Date: Mar 2022 |
A Phase 1/2 Study of DCC-3116 in Patients With RAS/MAPK Pathway Mutant Solid Tumors
Deciphera Pharmaceuticals, LLC
Non-Small Cell Lung Cancer
Advanced Solid Tumor
Metastatic Solid Tumor
This is a Phase 1/2, multicenter, open label, first in human (FIH) study of DCC-3116 as
monotherapy, and in combination with trametinib, binimetinib, or sotorasib in patients
with advanced or metastatic solid tumors with RAS/MAPK pathway mutation. The study
consists of 2 parts, a dose-escalation ph1 expand
This is a Phase 1/2, multicenter, open label, first in human (FIH) study of DCC-3116 as monotherapy, and in combination with trametinib, binimetinib, or sotorasib in patients with advanced or metastatic solid tumors with RAS/MAPK pathway mutation. The study consists of 2 parts, a dose-escalation phase, and an expansion phase. Type: Interventional Start Date: Jun 2021 |
Safe Accelerated Venetoclax Escalation in CLL
Dana-Farber Cancer Institute
Chronic Lymphocytic Leukemia
Small Lymphocytic Lymphoma
This research study is trying to determine which patients with newly diagnosed or
relapsed/refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma
(SLL), as grouped by their risk for tumor lysis syndrome (TLS), are able to safely
tolerate an accelerated, daily venetoclax dose ra1 expand
This research study is trying to determine which patients with newly diagnosed or relapsed/refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL), as grouped by their risk for tumor lysis syndrome (TLS), are able to safely tolerate an accelerated, daily venetoclax dose ramp-up rather than the standard approved schedule (5-week dose ramp-up). The name of the study drug involved in this study is: - Venetoclax The following drugs may also be included in some participants treatment regimen: - Obinutuzumab - Rituximab Type: Interventional Start Date: Apr 2021 |
Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Childr1
Duke University
Coronavirus Infection (COVID-19)
Pulmonary Arterial Hypertension
Urinary Tract Infections in Children
Hypertension
Pain
The study investigators are interested in learning more about how drugs, that are given
to children by their health care provider, act in the bodies of children and young adults
in hopes to find the most safe and effective dose for children. The primary objective of
this study is to evaluate the PK1 expand
The study investigators are interested in learning more about how drugs, that are given to children by their health care provider, act in the bodies of children and young adults in hopes to find the most safe and effective dose for children. The primary objective of this study is to evaluate the PK of understudied drugs currently being administered to children per SOC as prescribed by their treating provider. Type: Observational Start Date: Mar 2020 |
A Ph 2 Study of Glofitamab Alone or in Combination With Polatuzumab Vedotin or Atezolizumab in Rich1
Christine Ryan
Chronic Lymphocytic Leukemia
Richter's Transformation
This research is being done to evaluate Glofitamab by itself or in combination with
Polatuzumab Vedotin or Atezolizumab as possible treatments for Chronic Lymphocytic
Leukemia (CLL) that has transformed into Richter's Transformation (RT).
The names of the study drugs involved in this research stud1 expand
This research is being done to evaluate Glofitamab by itself or in combination with Polatuzumab Vedotin or Atezolizumab as possible treatments for Chronic Lymphocytic Leukemia (CLL) that has transformed into Richter's Transformation (RT). The names of the study drugs involved in this research study are: - Glofitamab (a T-cell bispecific humanized monoclonal antibody) - Obinutuzumab (a humanized glycoengineered type II anti-CD20 monoclonal antibody) - Polatuzumab vedotin (an antibody-drug conjugate) - Atezolizumab (a humanized immunoglobulin monoclonal antibody) - Tocilizumab (a recombinant, humanized, anti-human monoclonal antibody) Type: Interventional Start Date: Jan 2024 |
Polygenic Risk-based Detection of Subclinical Coronary Atherosclerosis and Intervention With Statin1
Massachusetts General Hospital
Coronary Artery Disease
The goal of this double-blind randomized controlled trial is to determine how treatment
with high intensity statin, low-dose colchicine, and their combination modulates
progression and composition of coronary atherosclerosis in individuals with high
polygenic risk for coronary artery disease. expand
The goal of this double-blind randomized controlled trial is to determine how treatment with high intensity statin, low-dose colchicine, and their combination modulates progression and composition of coronary atherosclerosis in individuals with high polygenic risk for coronary artery disease. Type: Interventional Start Date: Dec 2023 |
Defining the Role of Palliative carE for Patients With Hematologic Malignancies Undergoing Adoptive1
Massachusetts General Hospital
Hematologic Malignancy
Blood Cancer
Lymphoma
Leukemia
Multiple Myeloma
The goal of this study is to determine whether a palliative care intervention (PEACE) can
improve the quality of life and experiences of participants with Lymphoma, Leukemia, or
Multiple Myeloma receiving adoptive cellular therapy (ACT). After completion of an open
pilot, participants will be rando1 expand
The goal of this study is to determine whether a palliative care intervention (PEACE) can improve the quality of life and experiences of participants with Lymphoma, Leukemia, or Multiple Myeloma receiving adoptive cellular therapy (ACT). After completion of an open pilot, participants will be randomly assigned into one of two study intervention groups. The names of the study intervention groups involved in this study are: - Palliative care (PEACE) plus usual oncology care - Usual care (standard oncology care) Participation in this research study is expected to last for up to 2 years. It is expected that about 90 people will take part in this research study. Type: Interventional Start Date: Dec 2022 |
Deferoxamine for the Prevention of Cardiac Surgery-Associated Acute Kidney Injury
Brigham and Women's Hospital
Acute Kidney Injury
Multiple lines of evidence support a central role of iron in causing acute kidney injury
(AKI), including the finding that prophylactic administration of iron chelators
attenuates AKI in animal models. Patients undergoing cardiac surgery may be particularly
susceptible to iron-mediated kidney injur1 expand
Multiple lines of evidence support a central role of iron in causing acute kidney injury (AKI), including the finding that prophylactic administration of iron chelators attenuates AKI in animal models. Patients undergoing cardiac surgery may be particularly susceptible to iron-mediated kidney injury due to the profound hemolysis that often occurs from cardiopulmonary bypass. The investigators will test in a phase 2, randomized, double-blind, placebo-controlled trial whether prophylactic administration of deferoxamine decreases the incidence of AKI following cardiac surgery. Type: Interventional Start Date: Apr 2021 |
Use of Ketosis in Modulating Metabolic Pathways in Bipolar Disorder
Stony Brook University
Bipolar Disorder
Bipolar Disorder Type 1
The goal of this clinical trial is to test how specific components of diet affect brain
function and behavior for individuals with bipolar. The main question it aims to answer
is how glucose and ketones each affect the brain's response to risk and reward.
Participants will be asked to provide blood1 expand
The goal of this clinical trial is to test how specific components of diet affect brain function and behavior for individuals with bipolar. The main question it aims to answer is how glucose and ketones each affect the brain's response to risk and reward. Participants will be asked to provide blood (to assess baseline measures of how the body uses energy), and then to receive two MRI scan sessions, on separate days. During each MRI scan session, participants will play three games, from which they can win money, before and after drinking glucose (on one day) or ketones (on the other day). Investigators will compare individuals with and without bipolar to test whether the two groups differ in how their brains use energy, and to test how the brain's use of energy affects behavior. Type: Interventional Start Date: Jan 2024 |
A Study to Test How Well Different Doses of BI 3706674 Are Tolerated by People With Advanced Cancer1
Boehringer Ingelheim
Solid Tumor, KRAS Mutation
This study is open to adults with advanced cancer in the stomach and oesophagus. This is
a study for people for whom previous treatment was not successful or no treatment exists.
In this study, BI 3706674 is given to humans for the first time.
The purpose of this study is to find a suitable dose o1 expand
This study is open to adults with advanced cancer in the stomach and oesophagus. This is a study for people for whom previous treatment was not successful or no treatment exists. In this study, BI 3706674 is given to humans for the first time. The purpose of this study is to find a suitable dose of BI 3706674 that people with advanced cancer can tolerate when taken alone. Another purpose is to check whether BI 3706674 can make tumours shrink. BI 3706674 blocks growth signals and may prevent the tumour from growing. Participants take BI 3706674 as a tablet when starting treatment. Different doses of BI 3706674 are tested during this study. If there is benefit for the participants and if they can tolerate it, the treatment is given up to the maximum duration of the study. During this time, participants visit the study site regularly. The total number of visits depends on how they respond to and tolerate the treatment. Doctors record any unwanted effects and regularly check the general health of the participants. Type: Interventional Start Date: Oct 2023 |
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