Systemic Anti-Cancer Therapy Dose Modifications for Individuals With Duffy Null Phenotype
NCT07341867 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 90
Last updated 2026-01-14
Summary
This study is comprised of a main study, an observational study, and optional survey studies. The main study is being done to see whether using Duffy null specific treatment dosing guidelines can reduce or delay dose modifications and avoid neutropenic fever (fever in the setting of low neutrophils) for people with Duffy null phenotype receiving treatment for multiple myeloma or triple negative breast cancer. The observational study is to collect dose modification and neutropenic fever information on patients who do not have the Duffy null phenotype and receive the same standard of care regimens to see if there are differences in dose modifications and neutropenic fever between the two groups. The survey studies seek to understand general health experiences and preferences and experiences specific to people with Duffy null phenotype.
Study Drugs Include:
* Daratumumab
* lenalidomide
* bortezomib
* dexamethasone
* carboplatin
* paclitaxel
* pembrolizumab
* cyclophosphamide
* doxorubicin
Conditions
- Multiple Myeloma
- Triple Negative Breast Cancer
- Duffy Blood Group, Chemokine Receptor Gene Mutation
- Duffy Blood Group, Chemokine Receptor Gene C.-67T>C
Interventions
- DRUG
-
Tablet, taken orally
- DRUG
-
Intravenous infusion
- DRUG
-
Tablet, taken orally
- DRUG
-
Intravenous infusion
- DRUG
-
Intravenous infusion
- DRUG
-
Intravenous infusion
- DRUG
-
Intravenous infusion
- DRUG
-
Intravenous infusion
- DRUG
-
Doxorubicin
Intravenous infusion
Sponsors & Collaborators
-
Andrew Hantel, MD
lead OTHER
Principal Investigators
-
Andrew Hantel, MD · MD
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-06-30
- Primary Completion
- 2028-03-31
- Completion
- 2029-03-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
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