Study of CD133KDEL Toxin in the Treatment for Solid Tumors

NCT02845414 | Withdrawn Phase 1 FDA Drug

• 1 other identifier: 2016LS026
• Study Type: interventional
• Target: N/A
• Locations: 1 country
• Sites: 1

Brief Summary

This is a single center, phase I dose escalation study designed to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) of deimmunized CD133KDEL (dCD133KDEL), a ligand-directed, deimmunized pseudomonas toxin against CD133, in patients with advanced, previously treated, refractory solid tumors.

Conditions

Solid Tumors

Outcome Measures

Primary Outcomes (1)

• Maximum tolerated dose (MTD)

  Maximum tolerated dose (MTD)

  Day 28

Secondary Outcomes (2)

• Dose Limiting Toxicity (DLT)

  21 days after the first dose of dCD133KDEL

• Tumor response defined as partial and complete response according to RECIST 1.1 criteria, with its 95% confidence interval

  Disease assessment between days 29, 30, 31, 32, 33. Follow up for disease response every weeks 6, 7 ,8 ,9, 10,11,12

Study Arms (1)

Intravenous Infusion of dCD133KDEL

EXPERIMENTAL

Drug: CD133KDEL (dCD133KDEL)

Interventions

CD133KDEL (dCD133KDEL) DRUG

Patients will receive dCD133KDEL at the assigned dose level via a 30-minute intravenous infusion on days 1, 3, 5, 8, 10 and 12 (total of 6 doses) of a 28-day cycle.

Intravenous Infusion of dCD133KDEL

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Pathologically or cytologically confirmed, metastatic or unresectable solid tumor malignancy.
• Measurable or evaluable disease per RECIST 1.1 criteria (Appendix II), or modified RECIST criteria for mesothelioma (Appendix II).
• At least 1 prior line of systemic therapy considered standard for the malignancy, and for which no standard therapies exist. Prior systemic chemotherapy, immunotherapy, biological therapy, radiation therapy and/or surgery are allowed before the first dose of dCD133KDEL with the following restrictions:
• At least 14 days since any systemic therapy.
• At least 28 days since any experimental therapy.
• At least 14 days since any radiation therapy.
• At least 28 days since any major surgery, defined as a surgery involving a risk to the life of the patient, specifically, an operation upon an organ within the cranium, chest, abdomen, or pelvic cavity.
• Recovered from the acute toxic effects (≤ grade 1, CTCAE v4.0) of previous cancer treatment prior to study registration.
• ECOG performance status 0 or 1 (Appendix III).
• Adequate organ function within 14 days of study registration, defined as follows System Parameter Laboratory Value Hematologic Absolute neutrophil count (ANC) ≥1.5 x 10\^9 /L Hemoglobin\* 9 g/dL Platelets\* ≥100 x 10\^9 /L Hepatic Total bilirubin \< 2 x ULN\^ ALT \< 2 x ULN\^ Renal Serum creatinine \< 1.5 mg/dL OR estimated GFR \>50 by modified Cockcroft-Gault (\* Patient may not have had a transfusion within 7 days
• \^ Upper limit of institutional normal.)
• Albumin ≥ 3.0 gm/dL within 14 days of study registration.
• Adequate cardiac function, defined as an ejection fraction ≥40% on transthoracic echocardiogram done within 14 days of study registration.
• QT/QTc interval ≤ 450 milliseconds within 14 days of study registration. If this screening EKG demonstrates a QT/QTc interval \> 450 milliseconds, a second screening EKG will be done within 7 days to document that the QT prolongation is persistent. The patient will be eligible if the second screening EKG shows a QT/QTc interval ≤ 450 milliseconds but will require additional EKGs during the study period as outlined in section 6.1.2.
• Adequate pulmonary function, defined as resting oxygen saturation ≥ 90% on room air and/or pulmonary function tests (PFT) showing corrected DLCO \>50% and FEV1 ≥ 2 liters or ≥ 60% of predicted. PFT testing is required within 28 days of study registration only if the patient is symptomatic or prior known impairment is present.

You may not qualify if:

• Known active CNS metastases or neurological symptoms possibly related to CNS metastases, spinal cord compression, or evidence of leptomeningeal disease. Patients with a history of brain metastases who have undergone whole brain radiation or gamma knife treatment ≥ 28 days prior to registration, whose metastases are documented as stable or resolved at the time of screening by brain MRI (or head CT with contrast for those who are intolerant of MRI), and do not require ≥10 mg of prednisone equivalent for symptom management related to the brain metastases, are eligible.
• Known uncontrolled cardiac arrhythmias, electrocardiographic evidence of acute ischemia or active conduction system abnormalities within 28 days of registration.
• Uncontrolled intercurrent illness or psychiatric illness/social situations that would limit compliance with study requirements.
• History of any one or more cardiovascular conditions within 12 weeks of study registration
• cardiac angioplasty or stenting
• myocardial infarction
• unstable angina
• coronary artery bypass graft surgery
• symptomatic peripheral vascular disease
• Class III or IV congestive heart failure, as defined by the New York Heart Association (NYHA, Appendix IV)
• transient ischemic attack and/or cerebrovascular accident
• History of another malignancy other than non-melanoma skin cancer or treated carcinoma in situ, unless documented to be disease free for at least 3 years.
• History of allergic reaction or sensitivity to compounds of similar chemical or biological composition to dCD133KDEL, or any of the components of dCD133KDEL (i.e. Polysorbate 80).
• Pregnant or breastfeeding women, or women intending to become pregnant. Females of child bearing potential must have a negative serum pregnancy test within 14 days of study registration.
• Prior toxin-directed therapy

Sponsors & Collaborators

• Masonic Cancer Center, University of Minnesota: lead

Study Sites (1)

Masonic Cancer Center at University of Minnesota

Minneapolis, Minnesota, 55455, United States

Location

Study Officials

• Naomi Fujioka, MD

  University of Minnesota

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 18, 2016
• First Posted: July 27, 2016
• Study Start: December 1, 2018
• Primary Completion: January 1, 2022
• Study Completion: January 1, 2022
• Last Updated: October 3, 2018

Record last verified: 2018-10

Locations

US (1)