David J. Park, MD | Fullerton, CA

Dr. David Park, MD

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Providence Medical Foundation

Studies Pancreatic Cancer
Studies Lung Cancer
23 reported clinical trials
38 drugs studied

Area of expertise

1

Pancreatic Cancer

David Park, MD has run 8 trials for Pancreatic Cancer. Some of their research focus areas include:

Stage IV
EGFR positive
KRAS positive
2

Lung Cancer

David Park, MD has run 5 trials for Lung Cancer. Some of their research focus areas include:

Stage IV
Stage III
EGFR positive

Affiliated Hospitals

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Providence Medical Foundation

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Providence St. Jude Medical Center

Clinical Trials David Park, MD is currently running

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Supportive Care Models

for Cancer

This cluster-randomized comparative effectiveness trial compares a technology-based supportive cancer care (SCC) approach with a redesigned team-based supportive cancer care (SCC) approach.

Recruiting

1 award

N/A

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N-803 + PD-L1 t-haNK + Bevacizumab

for Glioblastoma

This study consists of 2 portions. The phase 2 portion is an open-label, single-arm study to evaluate the safety and efficacy of NAI, PD-L1 t-haNK, and bevacizumab combination therapy in participants with recurrent or progressive GBM. The phase 2B portion is an open-label, randomized study to evaluate the efficacy and safety for the following 2 experimental arms in participants with recurrent or progressive GBM: NAI, bevacizumab, and TTFields combination therapy (Arm A) or NAI, PD-L1 t-haNK, bevacizumab, and TTFields combination therapy (Arm B). Phase 2 Treatment for all enrolled participants will consist of repeated cycles of 28 days for a maximum treatment period of 76 weeks (19 cycles) as follows: Every 2 weeks (Days 1 and 15 of a 28-day cycle) Fourteen (14) participants were enrolled in the phase 2 portion of this study as of the date of this v02 protocol. No additional participants will be administered therapy in phase 2. Phase 2B Participants will be randomized 1:1 to 1 of 2 experimental arms (Arm A or Arm B). Treatment for all enrolled participants will consist of repeated 8-week cycles for a maximum treatment period of up to 80 weeks (10 cycles). Experimental Arm (A): Every 2 weeks (Days 1, 15, 29, and 43 of an 8-week cycle) Up to twenty (20) participants will be randomized in phase 2B (up to 10 participants/arm. Duration of Treatment: Participants will receive study treatment for up to 76 weeks during phase 2 (up to 19 repeated 28-day cycles) and for up to 80 weeks (up to 10 repeated 8-week cycles) during phase 2B or until they report unacceptable toxicity (not corrected with dose reduction), withdraw consent, or if the Investigator feels it is no longer in the participant's best interest to continue treatment. Treatment may also be discontinued if the participant has confirmed PD per iRANO, unless the participant is clinically stable and is considered potentially deriving benefit per Investigator's assessment. Duration of Follow-up: Participants who discontinue study treatment should remain in the study for follow-up. Participants should be followed for collection of survival status, posttreatment therapies (phase 2 and phase 2B), and medical history (phase 2B only) every 12 weeks (± 2 weeks) for the first 2 years then yearly thereafter for an additional 3 years. The maximum duration of follow-up is 5 years (260 weeks).

Recruiting

1 award

Phase 2

4 criteria

More about David Park, MD

Clinical Trial Related

3 years of experience running clinical trials · Led 23 trials as a Principal Investigator · 4 Active Clinical Trials

Treatments David Park, MD has experience with

  • ExoFlo
  • Bevacizumab
  • NovoTTF-200T
  • NovoTTF-100L(P)
  • Nab Paclitaxel
  • Gemcitabine

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