Dose-Escalation and Expansion Trial of NC-6300 in Patients With Advanced Solid Tumors or Soft Tissue Sarcoma

Solid Tumor Clinical Trial

Official title:

A Phase 1b/2 Dose-Escalation and Expansion Trial of NC-6300 (Nanoparticle Epirubicin) in Patients With Advanced Solid Tumors or Advanced, Metastatic, or Unresectable Soft Tissue Sarcoma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03168061
• Other study ID #: NC-6300-001
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: June 30, 2017
• Est. completion date: July 2020

Study information

• Verified date: February 2020
• Source: NanoCarrier Co., Ltd.
• Contact: Amanda Knight
• Phone: +1 919 443 3476
• Email: aknight[@]cato.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this study is to find the highest tolerated dose of NC-6300 that can be given to patients with advanced solid tumors or soft tissue sarcoma. The safety and tolerability of the drug will also be studied.

Description:

The first part of the study will determine the maximum tolerated dose (MTD), dose-limiting toxicities (DLTs), and the recommended Phase 2 (RPII) dose of NC-6300. The second part of the study will assess the activity and tolerability of NC-6300 in patients with soft tissue sarcoma.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 150
• Est. completion date: July 2020
• Est. primary completion date: July 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• (Part 1 only) Have a histologically/cytologically confirmed diagnosis of advanced solid tumor, including sarcoma that is refractory to standard therapy. (Part 2 only) Have a histologically confirmed diagnosis of advanced, unresectable, or metastatic soft tissue sarcoma not amenable to curative treatment with surgery or radiotherapy.

• Cohort 1: First-line soft tissue sarcoma of intermediate or high grade. Adjuvant or neoadjuvant chemotherapy allowed if no tumor recurrence for at least 12 months since the last measurement, beginning or end of last chemotherapy.

• Cohort 2: Soft tissue sarcoma of intermediate or high grade with evidence of disease progression by either CT or MRI scan, or clinical judgment on or after the last cancer therapy within 6 months prior to the start of study treatment. Relapsed or refractory (lack of response) to =1 course of systemic therapy regimen(s), excluding adjuvant or neoadjuvant chemotherapy, and is incurable by either surgery or radiation. Patients who have previously received anthracyclines are eligible if cumulative exposure is <375 mg/m2 for doxorubicin and liposomal doxorubicin or <675 mg/m2 for EPI.

• Have measurable disease per RECIST v.1.1.

• Have an ECOG performance status of 0 to 1.

• Have adequate bone marrow reserve defined as:

• Absolute neutrophil count of at least 1.5 × 109/L,

• Platelet count of at least 100 × 109/L, and

• Hemoglobin level of at least 10 g/dL (transfusion is allowed to achieve hemoglobin level of at least 10 g/dL).

• Have adequate liver function defined as:

• Total serum bilirubin <1.5 × ULN and

• ALT and AST <2.5 × ULN or, in patients with documented hepatic metastasis, =5.0 × ULN.

• Have adequate heart function defined as:

• LVEF of at least 50%

• Baseline QTc =470 msec and no previous history of QT prolongation while taking other medications.

• Have adequate renal function defined as a creatinine clearance =50 mL/minute (calculated according to the formula of Cockcroft and Gault 1976) or serum creatinine <1.5 mg/dL.

• Have reasonably recovered from preceding major surgery as judged by the investigator or have had no major surgery within 4 weeks prior to Day 1 treatment.

• Have stopped previous anticancer therapy for at least 2 weeks or 5 half-lives (whichever is longer) if the immediate prior regimen included only chemotherapy; or 4 weeks or 5 half-lives (whichever is longer) from any therapy with therapeutic biologics and from any type of investigational therapy.

• Women of childbearing potential are will to agree to use 1 of the study defined effective methods of birth control from the time of study entry to 60 days after the final study drug administration

• Women of childbearing potential must have a negative urine pregnancy test at screening, and

• Male patients must use highly effective contraception methods consisting of 2 forms of birth control (at least 1 of which must be a barrier method) starting at screening and continuing throughout the study period and for 60 days after the final study drug administration.

Exclusion Criteria:

• Prior exposure to >375 mg/m2 of doxorubicin or liposomal doxorubicin or =675 mg/m2 of EPI.

• Palliative surgery and/or radiation treatment within 30 days prior to date of screening visit.

• (Part 2 only) Current evidence/diagnosis of alveolar soft part sarcoma, extraskeletal myxoid chondrosarcoma, rhabdomyosarcoma, osteosarcoma, gastrointestinal stromal tumor, dermatofibrosarcoma (unless transformed to fibrosarcoma), Ewing's sarcoma, Kaposi's sarcoma, mixed mesodermal tumor, or clear cell sarcomas.

• Evidence of central nervous system metastasis and have not received prior definitive therapy for their lesions.

• Are unable to receive anthracycline therapy due to previous toxicity.

• Have unresolved toxicity from prior radiation, chemotherapy, or other targeted treatment, including investigational treatment, with the exception of alopecia and =Grade 1 peripheral neuropathy according to the NCI CTCAE v4.03. Clinical judgment by the investigator is allowed to determine if Grade 1 fatigue at screening is residual toxicity from prior treatment or is a symptom of the patient's general condition or disease. The investigator and Medical Monitor will discuss the eligibility of patients with baseline toxicity.

• Have a history of thrombocytopenia with complications including hemorrhage or bleeding of =Grade 2 per NCI CTCAE v4.03 that required medical intervention or have any hemolytic condition or coagulation disorder that would make participation unsafe in the opinion of the investigator.

• Have known hypersensitivity to anthracycline compounds or any excipient in NC-6300.

• Have uncontrolled diabetes or have hypertension requiring more than 3 medications for control of hypertension.

• Have an active, clinically significant serious infection requiring intravenous treatment with antibiotics, antivirals, or antifungals.

• Have signs or symptoms of organ failure, major chronic illnesses other than cancer, or any concomitant medical or social condition that, in the opinion of the investigator, make it undesirable for the patient to participate in the study or that could jeopardize compliance with the protocol.

• Have experienced any of the following within the 6-month period prior to screening:

angina pectoris, coronary artery disease or cerebrovascular accident, transient ischemic attack, cardiac failure with known ejection fraction less than 40%, or severe uncontrolled ventricular arrhythmia.

Related Conditions & MeSH terms

• Metastatic Sarcoma
• Sarcoma
• Soft Tissue Sarcoma
• Solid Tumor

Intervention

Drug:
• NC 6300
Part 1: NC-6300 at escalating doses starting at a fixed dose Part 2: NC-6300 at the RPII dose

Locations

Country	Name	City	State
United States	Montefiore Medical Center	Bronx	New York
United States	University of North Carolina at Chapel Hill	Chapel Hill	North Carolina
United States	City of Hope National Medical Center	Duarte	California
United States	Duke Cancer Institute	Durham	North Carolina
United States	Comprehensive Cancer Centers of Nevada - USOR	Las Vegas	Nevada
United States	Sarcoma Oncology Research Center, LLC.	Santa Monica	California
United States	University of California Los Angeles	Santa Monica	California

Sponsors (1)

Lead Sponsor	Collaborator
NanoCarrier Co., Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Ceoi	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	Cmax	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	Tmax	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	AUC	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	t1/2	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	Kel	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	CL	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	Vd	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Other	Ctrough	To characterize the pharmacokinetics of NC-6300.	through study completion, average 1 year
Primary	MTD dose of NC-6300		up to 7 cycles (21 days/cycle)
Primary	RPII dose of NC-6300		up to 7 cycles (21 days/cycle)
Secondary	Safety as measured by incidence and severity of TEAEs and laboratory anomalies	To evaluate the overall safety and tolerability of NC-6300 when administered as a single agent	through study completion, average 1 year
Secondary	Change in quality of life as measured by EORTC QLQ-C30	To evaluate the change in health-related quality of life following NC-6300 administration	through study completion, average 1 year