An Open-Label, Dose-Finding and Proof of Concept Study of the PD-L1 Probody Therapeutic , CX-072, as Monotherapy and in Combination With Yervoy (Ipilimumab) or With Zelboraf (Vemurafenib) in Subjects With Advanced or Recurrent Solid Tumors or Lymphomas

Trial Profile

An Open-Label, Dose-Finding and Proof of Concept Study of the PD-L1 Probody Therapeutic , CX-072, as Monotherapy and in Combination With Yervoy (Ipilimumab) or With Zelboraf (Vemurafenib) in Subjects With Advanced or Recurrent Solid Tumors or Lymphomas

Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 25 Sep 2017

At a glance

  • Drugs CX 072 (Primary) ; Ipilimumab (Primary) ; Vemurafenib (Primary)
  • Indications Lymphoma; Solid tumours
  • Focus Adverse reactions; First in man; Proof of concept
  • Acronyms PROCLAIM-CX-072
  • Sponsors CytomX Therapeutics
  • Most Recent Events

    • 12 Sep 2017 Trial design of the study presented at the 42nd European Society for Medical Oncology Congress.
    • 08 Sep 2017 According to a CytomX Therapeutics media release, trial design will be presented at at the European Society for Medical Oncology Annual Meeting.
    • 07 Aug 2017 According to a CytomX Therapeutics media release, the patient enrollment has been initiated for CX-072 in combination with Yervoy (ipilimumab) and Zelboraf (vemurafenib) arms . Also, enrollment for monotherapy dose escalation arm is expected to be complete in second half 2017. An expansion cohort of this study, to evaluate CX-072 as monotherapy, is expect to begin enrolling patients in first half of 2018.
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