First Line Bio-immunotherapy With Thymosin Alpha 1 in Patients With Sensitizing EGFR Mutation Positive Non Small Cell Lung Cancer Who Are Taking Standard of Care Therapy

NCT02906163 | Unknown Phase 1 DMC

• 1 other identifier: SCI-Ta1-NSCLC-P1/2-001
• Study Type: interventional
• Target: 188
• Locations: 1 country
• Sites: 5

Brief Summary

Phase I: evaluate the safety and tolerability two different dosing regimens of Thymosin alpha 1 in patients with advanced EGFR mutation positive NSCLC on Standard of Care (SoC) therapy. Phase II: evaluate the efficacy in terms of PFS of Thymosin alpha 1 in patients with advanced EGFR mutant NSCLC taking SoC as compared to SoC alone.

Conditions

EGFR Mutation Positive Non Small Cell Lung Cancer

Keywords

EGFR mutation positive; Thymosin Alpha 1; Tyrosine Kinase inhibitor; Thymalfasin; Non Small Cell Lung Cancer

Outcome Measures

Primary Outcomes (2)

• Number of treatment-related adverse events

  Up to 4 months

• PFS

  Up to12 months

Study Arms (3)

Thymalfasin biw plus SoC (tyrosine kinase inhibitor)

EXPERIMENTAL

Twice weekly thymalfasin

Drug: Thymalfasin (Thymosin alpha 1, Ta1); Drug: SoC (tyrosine kinase inhibitor)

Thymalfasin plus SoC (tyrosine kinase inhibitor)

EXPERIMENTAL

5 times a week thymalfasin

Drug: Thymalfasin (Thymosin alpha 1, Ta1); Drug: SoC (tyrosine kinase inhibitor)

SoC (tyrosine kinase inhibitor)

ACTIVE COMPARATOR

12 months

Drug: SoC (tyrosine kinase inhibitor)

Interventions

Thymalfasin (Thymosin alpha 1, Ta1) DRUG

In Phase I patients will be randomized to one of two different dosing regimens of Thymosin alpha 1 for a treatment duration of 4 months. At the completion of Phase I, data will be reviewed and a single dosing regimen will be carried forward into Phase II.

Also known as: ZADAXIN

Thymalfasin biw plus SoC (tyrosine kinase inhibitor); Thymalfasin plus SoC (tyrosine kinase inhibitor)

SoC (tyrosine kinase inhibitor) DRUG

In Phase II patients will be randomized to SoC or Thymosin alpha 1 plus SoC for treatment duration of 12 months. All patients will be followed for approximately 18 months.

Also known as: afatinib, gefitinib, erlotinib

SoC (tyrosine kinase inhibitor); Thymalfasin biw plus SoC (tyrosine kinase inhibitor); Thymalfasin plus SoC (tyrosine kinase inhibitor)

Eligibility Criteria

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

You may qualify if:

• Age 18 years or older
• Histological or cytological confirmation of NSCLC (may be from initial diagnosis of NSCLC or subsequent biopsy). Only patients with available tissue samples may be included in the study (see major details in section 8 for the minimum sample characteristics)
• Activating mutations of EGFRdiagnosis of Stage IIIB (with cytologically proven pleural effusion or pericardial effusion) or metastaticNSCLC, not amenable to curative surgery or radiotherapy
• Measurable disease by Response Evaluation Criteria In Solid Tumours (RECIST) in a lesion not previously irradiated or non-measurable disease (non measurable disease only for Phase I)
• Eastern Cooperative Oncology Group - performance status (ECOG-PS) 0-2
• Absolute neutrophil count (ANC) \> 1.5 x 109/liter (L) and platelets \> 100 x 109/L
• Bilirubin level either normal or \<1.5 x ULN
• AST (SGOT) and ALT (SGPT) \<2.5 x ULN (≤ 5 x ULN if liver metastases are present)
• Serum creatinine \<1.5 x ULN
• Effective contraception for both, male and female patients, if the risk of conception exists
• Provision of written informed consent to the analysis of biological markers (registration)

You may not qualify if:

• Prior therapy with Thymosin alpha-1
• Prior chemotherapy for relapsed and/or metastatic NSCLC. Neoadjuvant/adjuvant chemotherapy is permitted if at least 12 months has elapsed between the end of chemotherapy and randomisation.
• Prior treatment with Epidermal Growth Factor Receptor targeting small molecules or antibodies
• Radiotherapy within 14 days prior to drug administration, except as follows:
• Palliative radiation to organs other than chest may be allowed up to 2 weeks prior to drug administration, and
• Single dose palliative treatment for symptomatic metastasis outside above allowance to be discussed with sponsor prior to enrolling.
• Patients with previously diagnosed and treated CNS metastases or spinal cord compression may be considered if they have evidence of clinically stable disease (SD) (no steroid therapy or steroid dose being tapered) for at least 28 days
• Patients with toxicities that have not coming back (at least) to grade 1
• Pregnancy or suspected pregnancy
• Known severe hypersensitivity to TKI
• Other co-existing malignancies or malignancies diagnosed within the last 5 years with the exception of basal cell carcinoma or cervical cancer in situ
• Any evidence of clinically active interstitial lung disease (ILD) (patients with chronic, stable, radiographic changes who are asymptomatic or patients with uncomplicated progressive lymphangitic carcinomatosis need not be excluded)
• As judged by the investigator, any evidence of severe or uncontrolled systemic disease (e.g., unstable or uncompensated respiratory, cardiac, hepatic or renal disease)
• As judged by the investigator, any inflammatory changes of the surface of the eye
• Evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the study

Sponsors & Collaborators

• SciClone Pharmaceuticals: lead

Study Sites (5)

Azienda Sanitaria Locale Frosinone

Frosinone, Italy

Location

Istituto Nazionale dei Tumori

Milan, Italy

Location

Roma_Campus Bio-Medico

Rome, Italy

Location

Sant'Andrea Hospital

Rome, Italy

Location

Presidio Sanitario San Camillo

Torino, Italy

Location

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell Lung

Interventions

Thymalfasin; Trace amine-associated receptor 1; Tyrosine Kinase Inhibitors; Afatinib; Gefitinib; Erlotinib Hydrochloride

Condition Hierarchy (Ancestors)

Carcinoma, Bronchogenic; Bronchial Neoplasms; Lung Neoplasms; Respiratory Tract Neoplasms; Thoracic Neoplasms; Neoplasms by Site; Neoplasms; Lung Diseases; Respiratory Tract Diseases

Intervention Hierarchy (Ancestors)

Thymosin; Thymus Hormones; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Peptide Hormones; Peptides; Amino Acids, Peptides, and Proteins; Proteins; Protein Kinase Inhibitors; Enzyme Inhibitors; Molecular Mechanisms of Pharmacological Action; Pharmacologic Actions; Chemical Actions and Uses; Amides; Organic Chemicals; Quinazolines; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds

Study Officials

• Prof. Paolo Marchetti, MD

  S. Andrea Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Carlo Tomino, MD

CONTACT

carlotomino@gmail.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 29, 2016
• First Posted: September 19, 2016
• Study Start: October 1, 2016
• Primary Completion: December 1, 2019
• Study Completion: January 1, 2020
• Last Updated: September 19, 2016

Record last verified: 2016-09

Locations

IT (5)