MDA at Cooper University Health Care
Camden, New Jersey, 18103, United States
Location status: Recruiting
NCT Number: NCT07771803
Purpose/Specific Aims
The study will determine if there is a reduction in malignant cell burden when patients with relapsed and/or refractory acute myeloid leukemia (AML) or multiple myeloma (MM) consume tea made from the dried leaves of Annona muricata (Soursop).
The study goal is to determine the safety and anti-neoplastic efficacy of Annona muricata tea when taken in escalating frequency over a period of 21 days by patients with relapsed/refractory AML or MM for whom there are no standard therapeutic options.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Early Phase 1
Camden, New Jersey, 18103, United States
Location status: Recruiting
Acute Myeloid Leukemia (AML) and Multiple Myeloma (MM) are aggressive blood cancers. The median age of patients diagnosed with AML is between 65 and 70 years old and, despite recent advances in the management, most studies demonstrate less than 25% 5-year survival of patients over age 60. Likewise, although there have been extraordinary breakthroughs in the care of patients with MM, most patients with MM currently ultimately die of their disease.
Annona muricata is a plant that is native to Central and South America and found also in parts of the Caribbean, Europe, Asia and Africa. It is known by various names throughout the world (soursop, gravioloa, guanabana, paw paw, nangka balanda, and others). Seeds, fruit and leaves from the plant have all been used to treat a variety of diseases and ailments. The leaves are acuminate with a dark green upper surface and extracts include a variety of pharmacologically active classes of molecules (acetogenins, alkaloids, flavonoids) and a variety of their secondary products.
This pilot study is designed to determine if there is any signal of anti-neoplastic activity when patients with refractory/relapsed AML or MM with no standard therapeutic options available consume soursop tea.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The study is designed to test soursop tea therapy for 21 days, seven at each of 3 dose levels (1, 2 and 3 eight-ounce cups of soursop tea/d with each tea bag containing 1.5g of Shavuot leaves). Some patients may be on study for longer periods due to delays for toxicity observation. Only one delay will be allowed per patient. The patients will be assessed for leukemic or myeloma burden at the end of therapy. All patients will be monitored until resolution of tea-associated toxicities. All patients continuing soursop tea after the 21 days of treatment will continue to be followed for response and toxicity. If a specific intervention-associated CTCAE grade 2 or greater irreversible toxicity occurs in more than one person, the study will be stopped.
Time frame: From enrollment until end of treatment- 21 days
Reduction in AML cell percentage in blood or bone marrow e.g. (a >50% reduction in circulating leukemia cells) for the AML cohort. A 50 percent reduction in monoclonal protein or serum free light chains in the multiple myeloma cohort. Tea-associated toxicity will be graded by CTCAE v6 standards.
Time frame: From enrollment until end of treatment- 21 days
The assessments chosen are greatly simplified because of the pilot nature of the study.
Contact information is provided by the study sponsor or research team.
John Riehman-Murphy, RN
CONTACT
Roseann Freitag
CONTACT
Roger Strair
Other
Acronym: Soursop
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07486713
AML (Acute Myeloid Leukemia), Adenocarcinoma
Orange, California, United States
View Trial DetailsNCT07751991
AML (Acute Myeloid Leukemia), Hematologic Diseases
Grand Rapids, Michigan, United States
View Trial DetailsNCT07712848
AML (Acute Myeloid Leukemia), Hematologic Diseases
Kunming, Yunnan, China
View Trial DetailsNCT07347418
AML (Acute Myeloid Leukemia), Bone Marrow Diseases
Aurora, Colorado, United States
View Trial Details