Brea C. Lipe, M.D. | UR Medicine

Dr. Brea Lipe, MD

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University of Rochester

Studies Multiple Myeloma
Studies Relapse
9 reported clinical trials
17 drugs studied

Area of expertise

1Multiple Myeloma
Brea Lipe, MD has run 9 trials for Multiple Myeloma. Some of their research focus areas include:
Stage IV
HLA-A positive
2Relapse
Brea Lipe, MD has run 3 trials for Relapse. Some of their research focus areas include:
HLA-A positive

Affiliated Hospitals

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University Of Rochester
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University Of Rochester James P Wilmot Cancer Institute

Clinical Trials Brea Lipe, MD is currently running

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Curcumin + Piperine

for Prostate Cancer

This trial is testing if taking curcumin and piperine supplements can help prevent or slow down the progression of early-stage prostate cancer and certain blood conditions. The study will monitor a specific blood test to see if the disease is improving or getting worse. Curcumin, derived from the golden spice turmeric, has poor absorption in the body which can be improved when combined with piperine, a compound found in black pepper.
Recruiting1 award Phase 26 criteria
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Combination Therapies with Selinexor

for Multiple Myeloma

This study will independently assess the efficacy and safety of 11 combination therapies in 12 arms, in dose-escalation/-evaluation and expansion phases, for the treatment of patients with relapsed/refractory multiple myeloma (RRMM) and newly diagnosed multiple myeloma (NDMM). The combinations to be evaluated are: * Arm 1: Selinexor + dexamethasone + pomalidomide (SPd); enrollment complete * Arm 2: Selinexor + dexamethasone + bortezomib (SVd); enrollment complete * Arm 3: Selinexor + dexamethasone + lenalidomide (SRd) in RRMM; enrollment complete * Arm 4: Selinexor + dexamethasone + pomalidomide + bortezomib (SPVd); enrollment complete * Arm 5: Selinexor + dexamethasone + daratumumab (SDd); enrollment complete * Arm 6: Selinexor + dexamethasone + carfilzomib (SKd); enrollment complete * Arm 7: Selinexor + dexamethasone + lenalidomide (SRd) in NDMM; enrollment complete * Arm 8: Selinexor + dexamethasone + ixazomib (SNd); enrollment complete * Arm 9: Selinexor + dexamethasone + pomalidomide + elotuzumab (SPEd); enrollment complete * Arm 10: Selinexor + dexamethasone + belantamab mafodotin (SBd); enrollment complete * Arm 11: Selinexor + dexamethasone + pomalidomide + daratumumab (SDPd); enrollment complete * Arm 12: Selinexor + dexamethasone + mezigdomide (SMd); actively recruiting Selinexor pharmacokinetics: * PK Run-in (Days 1-14): Starting in protocol version 8.0, patients enrolled to any arm in the Dose Escalation Phase (i.e., Arm 4 \[SPVd\], Arm 6 \[SKd\], Arm 8 \[SNd\], Arm 9 \[SPEd\], Arm 10 \[SBd\], and Arm 11 \[SDPd\]) will also first be enrolled to a pharmacokinetics (PK) Run-in period until 9 patients have been enrolled to this period to evaluate the PK of selinexor before and after co-administration with a strong CYP3A4 inhibitor. This run-in period does not apply to Arm 12 (SMd).
Recruiting1 award Phase 1 & 222 criteria

More about Brea Lipe, MD

Clinical Trial Related6 years of experience running clinical trials · Led 9 trials as a Principal Investigator · 2 Active Clinical Trials
Treatments Brea Lipe, MD has experience with
  • Dexamethasone
  • Daratumumab
  • Bortezomib
  • Carfilzomib
  • Lenalidomide
  • Pomalidomide

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