EUCTR2014-002052-84-GB
Active, not recruiting
Not Applicable
An Exploratory Phase IIa Study to Investigate the Biological Activity of Oral FX125L in Adult Patients with Mild to Moderate Asthma
STX Pharma0 sitesJune 18, 2014
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- STX Pharma
- Status
- Active, not recruiting
- Last Updated
- 10 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Willing and able to give written informed consent and to comply with the requirements of the study.
- •2\. Male or female aged 18–77 years, inclusive.
- •3\. Body mass index 18–35 kg/m2, inclusive.
- •4\. Females of child\-bearing potential must be using an adequate and medically acceptable contraception method as outlined in the protocol.
- •5\. Females of child\-bearing potential must not be lactating or pregnant (negative serum beta\-human chorionic gonadotropin on Screening or urine pregnancy test at Day \-1 visit).
- •6\. Male patients must agree not to donate sperm, and to take appropriate precautions to avoid fathering a child, throughout the study and until 90 days after the end of treatment.
- •7\. Documented medical history of asthma at least 3 months prior to Screening, or equivalent that confirms the diagnosis meets this criteria.
- •8\. Forced expiratory volume in 1 second (FEV1\) \=90% of predicted at Screening and \=92% of predicted on (Day \-1\).
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
Exclusion Criteria
- •1\. Any condition, including findings in the medical history or in the pre\-study assessments, which, in the opinion of the Investigator, constitute a risk or contraindication for the participation of the subject in the study, or that could interfere with the study objectives, conduct, or evaluation including, but not limited to:
- •i. Any clinically significant abnormality in the results of screening safety laboratory tests.
- •ii. Positive test for drugs of abuse at screening or Day \-1\.
- •iii. Positive alcohol breath test at screening or Day \-1\.
- •iv. Positive results from serum tests for hepatitis B surface antigen (HbAg) (except if due to vaccination), hepatitis C (HCV), or human immunodeficiency virus (HIV).
- •v. History or presence of liver disease.
- •vi. History or presence of endocrine disorders or diseases affecting the hypothalamic\-pituitary\-adrenal axis, including acromegaly, growth hormone deficiency, adrenal insufficiency, Cushing’s syndrome, Grave’s Disease, Hashimoto’s Disease, uncontrolled diabetes mellitus, with the exception of idiopathic hypothyroidism in patients over the age of 60 years.
- •vii. History of hypofertility (males only)
- •viii. History of cancer in the preceding 5 years (except adequately treated basal cell carcinoma of the skin and squamous cell carcinoma in situ of the skin)
- •2\. History or presence of drug or alcohol abuse as defined by Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Active, not recruiting
Not Applicable
A study to investigate what effects FX125L (taken by mouth) has on adults with chronic inflammatory diseasesEUCTR2011-005036-26-GBFunxional Therapeutics Ltd
Completed
Phase 1
CytoMegaloVirus: Alternate donor Study of Pre-Emptive Cellular TherapyISRCTN75391842Cell Medica Ltd (UK)18
Active, not recruiting
Phase 1
A prospective phase I/II study to investigate the feasibility, safety and efficacy of IL-15 activated cytokine induced killer (CIK) cells in relapsing patients with acute leukemia or myelodysplastic syndromes after allogeneic stem cell transplantatiorelapsing acute leukemia, relapsing myelodysplastic syndromesMedDRA version: 17.0Level: LLTClassification code 10000835Term: Acute leukemiaSystem Organ Class: 100000004864MedDRA version: 17.0Level: HLTClassification code 10028536Term: Myelodysplastic syndromesSystem Organ Class: 100000004851Therapeutic area: Diseases [C] - Blood and lymphatic diseases [C15]EUCTR2013-005446-11-DEGoethe-University Frankfurt40
Active, not recruiting
Not Applicable
An exploratory, prospective phase II study to investigate progression-free survival, response and overall survival seen with pemetrexed/cisplatin and the role of thymidylate synthase expression.Advanced non-squamous non small cell lung cancerMedDRA version: 9.1Level: LLTClassification code 10025054Term: Lung cancer non-small cell stage IIIBMedDRA version: 9.1Level: LLTClassification code 10025055Term: Lung cancer non-small cell stage IVEUCTR2008-006709-18-GBEli Lilly and Company Limited68
Active, not recruiting
Not Applicable
An exploratory, prospective phase II study to investigate progression-free survival, response and overall survival seen with pemetrexed/cisplatin and the role of thymidylate synthase expression.Advanced non-squamous non small cell lung cancerMedDRA version: 9.1Level: LLTClassification code 10025054Term: Lung cancer non-small cell stage IIIBMedDRA version: 9.1Level: LLTClassification code 10025055Term: Lung cancer non-small cell stage IVEUCTR2008-006709-18-IEEli Lilly and Company Limited68