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NCT ID: NCT04975919 Active, not recruiting - Clinical trials for Refractory Acute Myeloid Leukemia

Venetoclax in Combination With Decitabine and Cedazuridine for the Treatment of Relapsed or Refractory Acute Myeloid Leukemia

Start date: September 29, 2021
Phase: Phase 2
Study type: Interventional

This phase II trial studies the effects of venetoxlax in combination with decitabine and cedazuridine in treating patients with acute myeloid leukemia that has come back (relapsed) or does not respond to treatment (refractory). Chemotherapy drugs, such as venetoclax and decitabine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Cedazuridine may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving venetoxlax in combination with decitabine and cedazuridine may help to control acute myeloid leukemia.

NCT ID: NCT04974047 Active, not recruiting - Clinical trials for Resectable Esophageal Squamous Cell Carcinoma

Study of Tislelizumab in Participants With Resectable Esophageal Squamous Cell Carcinoma

Start date: August 17, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the pathological complete response (pCR) in participants receiving tislelizumab plus chemotherapy/chemoradiotherapy as neoadjuvant treatment.

NCT ID: NCT04974021 Active, not recruiting - Clinical trials for Heart Failure With Reduced Ejection Fraction

Iron Intravenous Therapy in Reducing the Burden of Severe Arrhythmias in Heart Failure With Reduced Ejection Fraction

RESAFE
Start date: June 20, 2019
Phase:
Study type: Observational

An open label,single-center, non-interventional prospective study with the aim on investigating the effect of intravenous ferric carboxymaltose in restoring iron status and reducing the risk of severe arrhythmic events in participants with iron deficiency and a reduced ejection fraction (HFrEF).

NCT ID: NCT04972513 Active, not recruiting - Clinical trials for Cigarette Smoking-Related Carcinoma

Impact of E-cigarette Use on the Body

Start date: July 22, 2021
Phase:
Study type: Observational

This study examines how electronic (e)-cigarette use impacts the body, by studying both users and non-users of e-cigarettes. Early evidence indicates that e-cig users experience adverse health effects. Results of this study may help policy-makers develop standards for different types of tobacco.

NCT ID: NCT04971200 Active, not recruiting - Vitiligo Clinical Trials

Pilot Study Assessing the Effect of Tildrakizumab in Vitiligo

TILDVIT-1227
Start date: September 16, 2021
Phase: Early Phase 1
Study type: Interventional

Vitiligo is a common acquired depigmentation disorder affecting approximately 2% of the world population. The purpose of this pilot study is to evaluate the effect and the safety of Tildrakizumab in adult participants with vitiligo.

NCT ID: NCT04969887 Active, not recruiting - Clinical trials for Neuroendocrine Tumors

Combination Immunotherapy in Rare Cancers Under InvesTigation

MOST-CIRCUIT
Start date: August 3, 2021
Phase: Phase 2
Study type: Interventional

The four tumour streams that will be studied in this protocol are based on immunotherapy sensitive rare cancers from CA209-538 which will be further investigated under this protocol and divided into four groups: 1. Neuroendocrine cancers: Atypical bronchial carcinoid, neuroendocrine carcinoma and Grade 3 NETs independent of primary site (SCLC excluded) 2. Biliary tract cancers: Intrahepatic cholangiocarcinoma and gallbladder carcinoma 3. Gynaecological malignancies: Ovarian clear cell carcinoma, uterine clear cell carcinoma, uterine/ovarian carcinosarcoma, uterine leiomyosarcoma and vaginal/vulva squamous cell carcinoma 4. Mismatch repair protein deficient (MSI-H) cancers (excluding colorectal carcinoma). The role of immunotherapy is being defined in more common cancer types, however because of their rarity, the efficacy of immunotherapy for these cancers is poorly defined. This protocol provides an important opportunity to establish whether the combination of nivolumab & ipilimumab has efficacy in these cancers.

NCT ID: NCT04969315 Active, not recruiting - Clinical trials for Non Small Cell Lung Cancer

TT-10 as a Single Agent in Subjects With Advanced Selected Solid Tumors

Start date: June 23, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of orally administered TT-10 in subjects with advanced selected solid tumors. The dose escalation portion of the study will determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) of TT-10.

NCT ID: NCT04968119 Active, not recruiting - Clinical trials for Hematopoietic and Lymphoid Cell Neoplasm

Telehealth Exercise Platform to Reduce Frailty After Bone Marrow Transplant

Start date: July 12, 2021
Phase: N/A
Study type: Interventional

This clinical trial studies the feasibility of implementing a telehealth exercise platform to reduce frailty in patients after bone marrow transplant. The exercise program uses a telehealth platform (e.g. smart phones, tablets or computers) to view pre-recorded exercise videos on coordination, posture, stretching, balance and resistance/aerobic training. Physical activity may help to improve physical function, including frailty, after bone marrow transplant. Information from this trial may help researchers design future telehealth exercise routines for treating people with cancer.

NCT ID: NCT04967963 Active, not recruiting - Oral Surgery Clinical Trials

Surgical Management of Stage-2 MRONJ With Transplantation of HAM

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

Medication-related osteonecrosis of the jaw (MRONJ) is a drug adverse reaction and there is no consensus for the treatment of MRONJ. The aim of this study is to evaluate the mucosal coverage using HAM after sequestrectomy in patients with stage-2 MRONJ.

NCT ID: NCT04967196 Active, not recruiting - Metastatic Melanoma Clinical Trials

Ipilimumab and Nivolumab for the Treatment of Stage III-IV Unresectable Metastatic Melanoma

Start date: September 16, 2021
Phase: Phase 1
Study type: Interventional

This phase I trial identifies the best dose of ipilimumab that can be administered through the DoseConnectâ„¢ device followed by nivolumab in treating patients with stage III melanoma that cannot be removed by surgery (unresectable) or stage IV melanoma that has spread to other places in the body (metastatic). Immunotherapy with monoclonal antibodies, such as ipilimumab and nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.