Dr. Antonio Fojo, MD, PhD

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James J. Peters VA Medical Center, Bronx, NY

Studies Prostate Cancer
Studies Fanconi Anemia
3 reported clinical trials
5 drugs studied

Area of expertise

1

Prostate Cancer

Antonio Fojo, MD, PhD has run 3 trials for Prostate Cancer. Some of their research focus areas include:

Stage IV
MLH1 positive
MSH2 positive
2

Fanconi Anemia

Antonio Fojo, MD, PhD has run 1 trial for Fanconi Anemia. Some of their research focus areas include:

Stage IV
RAD51 positive
RAD51C positive

Affiliated Hospitals

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James J. Peters VA Medical Center, Bronx, NY

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Bronx VA Hospital

Clinical Trials Antonio Fojo, MD, PhD is currently running

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Pembrolizumab

for Prostate Cancer

The primary objective is to assess the activity and efficacy of pembrolizumab, a checkpoint inhibitor, in Veterans with metastatic castration-resistant prostate cancer (mCRPC) characterized by either mismatch repair deficiency (dMMR) or biallelic inactivation of CDK12 (CDK12-/-). The secondary objectives involve determining the frequency with which dMMR and CDK12-/- occur in this patient population, as well as the effects of pembrolizumab on various clinical endpoints (time to PSA progression, maximal PSA response, time to initiation of alternative anti-neoplastic therapy, time to radiographic progression, overall survival, and safety and tolerability). Lastly, the study will compare the pre-treatment and at-progression metastatic tumor biopsies to investigate the molecular correlates of resistance and sensitivity to pembrolizumab via RNA-sequencing, exome-sequencing, selected protein analyses, and multiplexed immunofluorescence.

Recruiting

2 awards

Phase 2

3 criteria

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Carboplatin vs Olaparib

for Prostate Cancer

This is an unblinded, randomized clinical study comparing the efficacy of DNA damaging chemotherapy using carboplatin, to standard of care therapy for patients who have metastatic castrate resistant prostate cancer. This trial will use olaparib or carboplatin as initial therapy with crossover to the alternate or second-line drug after first progression for patients with tumors containing BARD1, BRCA1, BRCA2, BRIP1, CHEK1, FANCL, PALB2, RAD51B, RAD51C, RAD51D, or RAD54L inactivating mutations. Participants are randomized (1:1) and receive either carboplatin (AUC 5, IV) every 21 days, first or olaparib taken orally (300 mg), twice daily in 28 day cycles, until intolerance, complete response, or progression by Prostate Cancer Working Group 3 (PCWG3) criteria. Participants then crossover from the first-line therapy to the second-line therapy with the opposite study medication and receive treatment to intolerance or progression (whichever is first). Enrolled participants will be allowed to crossover to second line therapy if they continue to meet initial eligibility criteria, and at least three weeks have elapsed since last administration of either carboplatin or olaparib. Throughout the study, safety and tolerability will be assessed. Progression will be evaluated with bone scan, CT of the abdomen/pelvis, or MRI and PSA as per PCWG3 criteria.

Recruiting

1 award

Phase 2

More about Antonio Fojo, MD, PhD

Clinical Trial Related

5 years of experience running clinical trials · Led 3 trials as a Principal Investigator · 2 Active Clinical Trials

Treatments Antonio Fojo, MD, PhD has experience with

  • Carboplatin
  • Olaparib
  • Pembrolizumab
  • Docetaxel
  • Radium-223

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