• Phone: 803-329-7772
  • Fax: 803-329-9821

Clinical trials are essential in the medical field as they allow for the evolution of the standards of care. Within the oncology specialty, these efforts are dedicated to advancing the methods of cancer prevention, detection, and treatment. Currently, our list of ongoing trials include:

Sponsor : Amgen
Protocol No:
20170758
Title:
A Prospectitve Observational Study to Estimate the Incidence of Febrile Neutropenia (FN) Among Subjects With Non-myeloid Malignancies at High Risk for FN and Receiving Neulasta (pegfilgrastim) Onpro kit or Other Physician Choice Options for Prophylaxis of FN
Diagnosis Requirements:
breast cancer, lung cancer, non-Hodgkin’s lymphoma, or prostate cancer
Ask your doctor about this trial if:
You are beginning a new chemotherapy regimen soon
Sponsor : Aptose Biosciences
Protocol No:
APTO-CG-806-01
Title:
A Phase 1 a/b trial to evaluate the safety and tolerability of CG-806 in patients with CLL/SLL or Non-Hodgkin’s Lymphomas
Diagnosis Requirements:
Non-Hodgkin’s lymphoma or chronic lymphocytic lymphoma
Ask your doctor about this trial if:
You have one of these conditions, have been in remission, and are now needing new treatment
Note: Involves investigational product
Sponsor : Aptose Biosciences
Protocol No:
APTO-CG-806-01
Title:
A Phase 1 a/b trial to evaluate the safety and tolerability of CG-806 in patients with CLL/SLL or Non-Hodgkin’s Lymphomas
Diagnosis Requirements:
Non-Hodgkin’s lymphoma or chronic lymphocytic lymphoma
Ask your doctor about this trial if:
You have one of these conditions, have been in remission, and are now needing new treatment
Note: Involves investigational product
Sponsor : Celgene Corporation
Protocol No:
ACE-536-MDS-002
Title:
A Phase 3, Open-label, Randomized Study to Compare the Efficacy and Safety of Luspatercept (ACE-536) versus Epoetin alfa for the Treatment of Anemia due to IPSS-R Very Low, Low or Intermediate Risk Myelodysplastic Syndromes (MDS) in ESA Naïve Subjects who require Red Blood Cell Transfusions.
Diagnosis Requirements:
A Phase 1 a/b trial to evaluate the safety and tolerability of CG-806 in patients with CLL/SLL or Non-Hodgkin’s Lymphomas
Ask your doctor about this trial if:
You receive red-blood cell transfusions, but have not received any EPO stimulating agents (i.e. Procrit)
Note: Involves investigational product
Sponsor: Paradigm Diagnostics Registry
Protocol No:
20170357
Title:
A Prospective Registry Study to Evaluate the Efficacy of Precision Molecular Testing in the Treatment of Advanced Solid Tumors
Note: Testing is done as part of standard of care. Once testing is completed, patient may be approached about enrolling in the voluntary registry

Please contact the Carolina Blood and Cancer Care Associates Clinical Research team with any questions, or if interested in any of these studies at (803)-329-7772 All clinical studies and trials run by Carolina Blood and Cancer Care Associates can be found at clinicaltrials.gov