Dr. Krisstina Gowin
Claim this profileGSK Investigational Site
Studies Multiple Myeloma
Studies Plasma Cell Neoplasm
4 reported clinical trials
5 drugs studied
Affiliated Hospitals
Clinical Trials Krisstina Gowin is currently running
Belantamab Mafodotin
for Multiple Myeloma
The purpose of this study is to assess the pharmacokinetics (PK), safety, and tolerability of belantamab mafodotin monotherapy in Relapsed/Refractory Multiple Myeloma (RRMM) participants with impaired hepatic function and in matched RRMM participants with normal hepatic function.
Recruiting1 award Phase 111 criteria
Belantamab Mafodotin
for Multiple Myeloma
Belantamab mafodotin is an antibody-drug conjugate (ADC) containing humanized anti- B-cell maturation antigen (BCMA) monoclonal antibody (mAb). Renal impairment is a major complication of multiple myeloma (MM) and the majority of MM participants is either at risk or already has renal dysfunction at initial diagnosis. The purpose of this study is to assess the pharmacokinetics (PK), safety, and tolerability of belantamab mafodotin monotherapy in participants with RRMM, who have had at least 3 lines of prior treatment (or at least 2 lines of prior treatment if ineligible for autologous stem cell transplantation ) and have either normal or impaired renal functions. The study will consist of two parts: part 1 will include participants with normal/mildly impaired renal function and severe renal impairment and part 2 will include participants with end-stage renal disease (ESRD), where participants are either not undergoing or require hemodialysis. Participants will be administered belantamab mafodotin at a dose of 2.5 milligram per kilogram (mg/kg) intravenously once in three weeks (Q3W) dosing in Part 1. Based on the Part 1 Safety/Pharmacokinetic (PK) data, Part 2 participants will be administered the dose of either 2.5 mg/kg or 1.9 mg/kg (or other adjusted dose). Participants will be treated with belantamab mafodotin monotherapy until confirmed disease progression, death, unacceptable toxicity, withdrawal of consent, or end of study, whichever occurs first. This study will include a screening phase, treatment phase, follow-up phase and a post analysis continued treatment (PACT) phase . The total duration of the study is approximately up to 48 months.
Recruiting1 award Phase 110 criteria
More about Krisstina Gowin
Clinical Trial Related3 years of experience running clinical trials · Led 4 trials as a Principal Investigator · 2 Active Clinical TrialsTreatments Krisstina Gowin has experience with
- Tai Chi Easy
- Delayed Yoga Intervention
- Immediate Yoga Intervention
- Belantamab Mafodotin
- Belantamab Mafodotin
Breakdown of trials Krisstina Gowin has run
Multiple Myeloma
Plasma Cell Neoplasm
Stem Cell Transplant Complications
Kidney Failure
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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 Krisstina Gowin specialize in?
Krisstina Gowin focuses on Multiple Myeloma and Plasma Cell Neoplasm. In particular, much of their work with Multiple Myeloma has involved treating patients, or patients who are undergoing treatment.
Is Krisstina Gowin currently recruiting for clinical trials?
Yes, Krisstina Gowin is currently recruiting for 2 clinical trials in Tucson Arizona. If you're interested in participating, you should apply.
Are there any treatments that Krisstina Gowin has studied deeply?
Yes, Krisstina Gowin has studied treatments such as Tai Chi Easy, Delayed yoga intervention, Immediate yoga intervention.
What is the best way to schedule an appointment with Krisstina Gowin?
Apply for one of the trials that Krisstina Gowin is conducting.
What is the office address of Krisstina Gowin?
The office of Krisstina Gowin is located at: GSK Investigational Site, Tucson, Arizona 85724 United States. This is the address for their practice at the GSK Investigational Site.
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.