SF1126 in Recurrent or Progressive SCCHN and Mutations in PIK3CA Gene and/or PI-3 Kinase Pathway Genes

Metastatic Squamous Neck Cancer With Occult Primary Squamous Cell Carcinoma Clinical Trial

Official title:

A Phase II Open Label Study of the PI3 Kinase (PI-3) Inhibitor, SF1126, in Patients With Recurrent or Progressive SCCHN and Mutations in PIK3CA Gene and/or PI-3 Kinase Pathway Genes

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02644122
• Other study ID #: 140904
• Status: Terminated
• Phase: Phase 2
• Start date: November 2016
• Est. completion date: December 2016

Study information

• Verified date: June 2018
• Source: University of California, San Diego
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to test the good and bad effects of an experimental drug called SF1126. This drug is being tested in patients whose cancer has not been controlled by available standard therapies and who have certain genes in their tumor.

SF1126 is a drug that inhibits a cell protein called phosphatidyl inositol 3 kinase (PI3K). PI3K is part of signaling pathway that tells cancer cells to grow, survive, invade and metastasize. PI3K also has an important role in the development of blood vessels that are required to support tumor growth. SF1126 is being developed by SignalRx Pharmaceuticals, Inc. It is considered an experimental drug because it is not approved by the FDA for any disease treatment.

Description:

SignalRx Pharmaceuticals has developed a pan isoform specific PI-3 inhibitor called SF1126 to treat patients with advanced or metastatic cancer. SF1126 is a conjugate that contains two components: SF1101 (the active drug) and SF1174 (an inactive tetrapeptide RGD targeting moiety)

Both components of SF1126 play key roles in the activity of the drug. SF1101 is a selective inhibitor of certain members of the phosphatidyl inositol 3-kinase (PI-3) family and SF1174 binds selectively to receptors known to be present on neovasculature supporting tumors and on some tumor cells themselves. These components result in a drug designed to be both selective in its activity and targeted in its delivery.

This is an open label Phase II study of SF1126 in adult patients with recurrent or refractory advanced SCCHN with PIK3CA mutation. Treatment cycles (28 days) will consist of SF1126 1110 mg/m2 administered intravenously (IV) twice per week (separated by at least three days) for the first four cycles and then once weekly for subsequent cycles.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 1
• Est. completion date: December 2016
• Est. primary completion date: December 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of recurrent or metastatic SCCHN or any site except lip, thyroid, salivary gland, or nasopharynx.

• No known FDA-approved therapy available that's expected to prolong survival by greater than 3 months.

• Tumors with at least one of the following known mutations in the PI-3K signaling pathway, via assays performed in a CLIA-approved setting (Foundation Medicine FoundationOne test will be used. This assay uses a cut-off of 5% allele fraction for mutations. Allele fraction will be requested on each sample):

1. PIK3CA,

2. PIK3CG,

3. PIK3R1, PIK3R5 and PIK3AP1 (regulatory subunits),

4. AKT and mTOR, or

5. PTEN Note: PIK3CA amplification is not eligible.

• Prior receipt of platinum-containing chemotherapy for recurrent/metastatic disease or a history of progression of disease within 6 months of receiving platinum as part of concurrent chemoradiation.

• Disease must not be amenable to potentially curative treatment..

• Has recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy.

• Myelosuppressive chemotherapy: At least 3 weeks since completion (6 weeks for nitrosourea)

• Biologic (anti-neoplastic agent): At least 14 days since completion of therapy with a biologic agent.

• Radiation (XRT):1 week must have elapsed from prior palliative XRT to non-target lesions.

• Adequate Bone Marrow Function Defined for all subjects (including status post SCT):

• Peripheral absolute neutrophil count (ANC) 1000/mm3; Note: must be >7 days from use of hematopoietic growth factor or 21 days from pegfilgastrim

• Platelet count 75,000/ mm3 (transfusion independent for >7 days)

• Hemoglobin 8.0 g/dL (may receive transfusions)

• Adequate Renal Function Defined As:

• Serum creatinine = 1.5 x institution's ULN (upper limit of normal), or

• Creatinine clearance 50 ml/min

• Adequate Liver and Pancreatic Function Defined As:

• Total bilirubin 1.5 x upper limit of normal, and

• ALT or AST 5 x upper limit of normal, and

• Albumin 2 g/dL

• Adequate Central Nervous System Function Defined As:

• Subjects with seizure disorder may be enrolled if on anticonvulsants and seizures are well controlled.

Exclusion Criteria:

• Brain metastases or spinal cord compression, unless treatment was completed at least 4 weeks before study entry, and stable without steroid treatment for at least 4 weeks.

• Evidence of severe or uncontrolled systemic diseases (e.g., unstable or uncompensated respiratory, cardiac [including life threatening arrhythmias], hepatic, or renal disease).

• Unresolved toxicity = CTCAE Grade 2 from previous anti-cancer therapy except alopecia or long-term radiation toxicity (radiation related toxicity 3 months or greater after radiation exposure).

• Presence of cardiac impairment defined as:

• Prior history of cardiovascular disease including heart failure that meets New York Hearth Association (NYHA) class III and IV definitions; OR

• History of myocardial infarction/active ischemic heart disease within one year of study entry; OR

• Uncontrolled dysrhythmias; OR

• Poorly controlled angina.

• Participation in a trial of an investigational agent within the prior 30 days.

• Pregnant or breast-feeding females.

• History of other malignancies except curatively excised carcinoma in situ of the cervix, non-melanomatous skin carcinoma or superficial bladder cancer or other solid tumors curatively treated with no evidence of disease for 3 years. Other cases will be reviewed and possibly allowed if discussed with and approved by the Principal Investigator.

• Patients receiving therapeutic doses of warfarin.

• Blood pressure greater than 170/90 or two standard deviations from normal based on age and weight nomogram on three separate measurements.

Related Conditions & MeSH terms

• Carcinoma, Squamous Cell
• Head and Neck Neoplasms
• Metastatic Squamous Neck Cancer With Occult Primary Squamous Cell Carcinoma
• Neoplasms, Unknown Primary

Intervention

Drug:
• SF1126

Locations

Country	Name	City	State
United States	UC San Diego Moores Cancer Center	La Jolla	California

Sponsors (2)

Lead Sponsor	Collaborator
Ezra Cohen	SignalRX Pharmaceuticals, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To Determine ORR	best response of PR or CR observed within 6 months of enrollment	6 months
Secondary	Number of Participants With Treatment-related Adverse Events		4 years
Secondary	To Assess the Effect of SF1126 on Time to Progression.		4 years
Secondary	To Assess the Effect of SF1126 on Overall Survival.		4 years
Secondary	To Assess Disease-related Patient-reported Outcomes Using the EORTC-QLQ-		4 years