Dr. Nina S. Kadan-Lottick

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MedStar Georgetown University Hospital

Expert in Tumors
Expert in Cancer
37 reported clinical trials
83 drugs studied

About Nina S. Kadan-Lottick

Education:

  • Obtained an MD from Johns Hopkins University School of Medicine.
  • Earned an MSPH from Johns Hopkins Bloomberg School of Public Health.

Experience:

  • Founded and serves as Medical Director of the HEROS Program at Yale University School of Medicine, dedicated to long-term childhood cancer survivors.
  • Holds the position of Director of the Survivorship Research Initiative at Georgetown Lombardi Comprehensive Cancer Center.
  • Works as a Pediatric hematologist-oncologist and research scientist, with a focus on survivorship research for long-term childhood cancer survivors.

Area of expertise

1Tumors
Global Leader
Nina S. Kadan-Lottick has run 17 trials for Tumors. Some of their research focus areas include:
Stage I
Stage II
Stage IV
2Cancer
Global Leader
Nina S. Kadan-Lottick has run 11 trials for Cancer. Some of their research focus areas include:
Stage I
Stage II
Stage IV

Affiliated Hospitals

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MedStar Georgetown University Hospital
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Yale University

Clinical Trials Nina S. Kadan-Lottick is currently running

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Genetic Testing-Directed Therapy

for Pediatric Cancer

This Pediatric MATCH screening and multi-sub-study phase II trial studies how well treatment that is directed by genetic testing works in pediatric patients with solid tumors, non-Hodgkin lymphomas, or histiocytic disorders that have progressed following at least one line of standard systemic therapy and/or for which no standard treatment exists that has been shown to prolong survival. Genetic tests look at the unique genetic material (genes) of patients' tumor cells. Patients with genetic changes or abnormalities (mutations) may benefit more from treatment which targets their tumor's particular genetic mutation, and may help doctors plan better treatment for patients with solid tumors or non-Hodgkin lymphomas.
Recruiting1 award Phase 214 criteria
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Inotuzumab Ozogamicin

for Acute Lymphoblastic Leukemia

This phase III trial studies whether inotuzumab ozogamicin added to post-induction chemotherapy for patients with High-Risk B-cell Acute Lymphoblastic Leukemia (B-ALL) improves outcomes. This trial also studies the outcomes of patients with mixed phenotype acute leukemia (MPAL), and B-lymphoblastic lymphoma (B-LLy) when treated with ALL therapy without inotuzumab ozogamicin. Inotuzumab ozogamicin is a monoclonal antibody, called inotuzumab, linked to a type of chemotherapy called calicheamicin. Inotuzumab attaches to cancer cells in a targeted way and delivers calicheamicin to kill them. Other drugs used in the chemotherapy regimen, such as cyclophosphamide, cytarabine, dexamethasone, doxorubicin, daunorubicin, methotrexate, leucovorin, mercaptopurine, prednisone, thioguanine, vincristine, and pegaspargase or calaspargase pegol 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. This trial will also study the outcomes of patients with mixed phenotype acute leukemia (MPAL) and disseminated B lymphoblastic lymphoma (B-LLy) when treated with high-risk ALL chemotherapy. The overall goal of this study is to understand if adding inotuzumab ozogamicin to standard of care chemotherapy maintains or improves outcomes in High Risk B-cell Acute Lymphoblastic Leukemia (HR B-ALL). The first part of the study includes the first two phases of therapy: Induction and Consolidation. This part will collect information on the leukemia, as well as the effects of the initial treatment, to classify patients into post-consolidation treatment groups. On the second part of this study, patients with HR B-ALL will receive the remainder of the chemotherapy cycles (interim maintenance I, delayed intensification, interim maintenance II, maintenance), with some patients randomized to receive inotuzumab. The patients that receive inotuzumab will not receive part of delayed intensification. Other aims of this study include investigating whether treating both males and females with the same duration of chemotherapy maintains outcomes for males who have previously been treated for an additional year compared to girls, as well as to evaluate the best ways to help patients adhere to oral chemotherapy regimens. Finally, this study will be the first to track the outcomes of subjects with disseminated B-cell Lymphoblastic Leukemia (B-LLy) or Mixed Phenotype Acute Leukemia (MPAL) when treated with B-ALL chemotherapy.
Recruiting2 awards Phase 3

More about Nina S. Kadan-Lottick

Clinical Trial Related7 years of experience running clinical trials · Led 37 trials as a Principal Investigator · 12 Active Clinical Trials
Treatments Nina S. Kadan-Lottick has experience with
  • Cyclophosphamide
  • Radiation Therapy
  • Doxorubicin Hydrochloride
  • Laboratory Biomarker Analysis
  • Cisplatin
  • Carboplatin

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Frequently asked questions

Do I need insurance to participate in a trial?
Almost all clinical trials will cover the cost of the ‘trial drug’ — so no insurance is required for this. For trials where this trial drug is given alongside an already-approved medication, there may be a cost (which your insurance would normally cover).
What does Nina S. Kadan-Lottick specialize in?
Nina S. Kadan-Lottick focuses on Tumors and Cancer. In particular, much of their work with Tumors has involved Stage I patients, or patients who are Stage II.
Is Nina S. Kadan-Lottick currently recruiting for clinical trials?
Yes, Nina S. Kadan-Lottick is currently recruiting for 6 clinical trials in Washington District of Columbia. If you're interested in participating, you should apply.
Are there any treatments that Nina S. Kadan-Lottick has studied deeply?
Yes, Nina S. Kadan-Lottick has studied treatments such as Cyclophosphamide, Radiation Therapy, Doxorubicin Hydrochloride.
What is the best way to schedule an appointment with Nina S. Kadan-Lottick?
Apply for one of the trials that Nina S. Kadan-Lottick is conducting.
What is the office address of Nina S. Kadan-Lottick?
The office of Nina S. Kadan-Lottick is located at: MedStar Georgetown University Hospital, Washington, District of Columbia 20007 United States. This is the address for their practice at the MedStar Georgetown University Hospital.
Is there any support for travel costs?
The coverage of travel expenses can vary greatly between different clinical trials. Please see more financial detail in the trials you’re interested to apply.