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Investigation of the Effect of Nintedanib on the Pharmacokinetics of a Combination of Ethinylestradiol and Levonorgestrel in Patients With Non-small Cell Lung Cancer

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ClinicalTrials.gov Identifier: NCT02751385
Recruitment Status : Terminated (Terminated- Study halted due to low recruitment.)
First Posted : April 26, 2016
Last Update Posted : January 18, 2018
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim

Brief Summary:
Investigate the effect of multiple oral doses of nintedanib on the single dose kinetics of a combination of ethinylestradiol and levonorgestrel (Microgynon®)

Condition or disease Intervention/treatment Phase
Carcinoma, Non-Small-Cell Lung Drug: Microgynon Drug: Nintedanib Phase 1

Detailed Description:
Purpose:

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 2 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Other
Official Title: A Phase I Trial to Investigate the Effect of Nintedanib on the Pharmacokinetics of a Combination of Ethinylestradiol and Levonorgestrel in Patients With Non-small Cell Lung Cancer
Actual Study Start Date : May 20, 2016
Actual Primary Completion Date : November 28, 2017
Actual Study Completion Date : November 28, 2017

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: All Patients
Microgynon alone in Period 1 then with Nintedanib in Period 2
Drug: Microgynon
Drug: Nintedanib



Primary Outcome Measures :
  1. AUC 0-tz (area under the concentration-time curve of ethinylestradiol before nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]
  2. AUC 0-tz (area under the concentration-time curve of levonorgestrel before nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]
  3. AUC 0-tz (area under the concentration-time curve of ethinylestradiol after continuous nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]
  4. AUC 0-tz (area under the concentration-time curve of levonorgestrel after continuous nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]
  5. Cmax (maximum measured concentration) of ethinylestradiol before nintedanib administration in plasma [ Time Frame: at week 3 ]
  6. Cmax (maximum measured concentration) of levonorgestrel before nintedanib administration in plasma [ Time Frame: at week 3 ]
  7. Cmax (maximum measured concentration) of ethinylestradiol after continuous nintedanib administration in plasma [ Time Frame: at week 3 ]
  8. Cmax (maximum measured concentration) of levonorgestrel after continuous nintedanib administration in plasma [ Time Frame: at week 3 ]

Secondary Outcome Measures :
  1. AUC0-infinity (area under the concentration-time curve of ethinylestradiol before nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]
  2. AUC0-infinity (area under the concentration-time curve of levonorgestrel before nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]
  3. AUC0-infinity (area under the concentration-time curve of ethinylestradiol after continuous nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]
  4. AUC0-infinity (area under the concentration-time curve of levonorgestrel after continuous nintedanib administration in plasma over the time interval from 0 to the time of the last quantifiable data point) [ Time Frame: at week 3 ]


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • Female patients 18 years or older at screening
  • Female patient is postmenopausal or surgically sterilised
  • Patient with locally advanced, metastatic or locally recurrent non-small cell lung cancer with histology of adenocarcinoma
  • Nintedanib (Vargatef®) is planned to be prescribed in accordance with the marketing authorisation (SmPC)
  • Signed and dated written informed consent in accordance with Good Clinical Practice (GCP) and local legislation prior to admission to the trial

Exclusion criteria:

  • Any contraindication to nintedanib (Vargatef®), ethinylestradiol or levonorgestrel (Microgynon®), as specified in the respective labels
  • Use of hormone containing contraceptives (including vaginal and intrauterine devices and including hormone replacement therapy) within 30 days prior to first administration of Microgynon®
  • Systemic use of drugs known to induce (e.g. rifampicin, St. John's Wort, carbamazepine) or to inhibit (e.g. azole antimycotics, macrolides) CYP3A4 within 7 days prior to first trial drug administration until last PK-sampling in the trial. Exception: allowed is the intake of corticosteroids as docetaxel (pre)medication
  • History of major thrombotic or clinically relevant major bleeding event in the past 6 months
  • Persistence of clinically relevant therapy related toxicities (i.e. > Common Terminology Criteria for Adverse Events [CTCAE] grade 2) from previous chemotherapy and/or radiotherapy
  • Treatment with other investigational drugs or treatment in another clinical trial within the past four weeks before start of therapy or concomitantly with this trial
  • Gastrointestinal disorders or abnormalities that would interfere with absorption of the trial drugs
  • Major surgery (major according to the investigator's assessment) performed within 4 weeks prior to first treatment within the trial and without complete wound healing
  • Patients who must or wish to continue the intake of restricted medications or any drug considered likely to interfere with the safe conduct of the trial
  • Patients unable to comply with the protocol
  • Previous enrolment in this trial

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02751385


Locations
Germany
Klinikum Chemnitz gGmbH
Chemnitz, Germany, 09116
Sponsors and Collaborators
Boehringer Ingelheim
Investigators
Study Chair: Boehringer Ingelheim Boehringer Ingelheim

Responsible Party: Boehringer Ingelheim
ClinicalTrials.gov Identifier: NCT02751385     History of Changes
Other Study ID Numbers: 1199.238
2015-005664-41 ( EudraCT Number )
First Posted: April 26, 2016    Key Record Dates
Last Update Posted: January 18, 2018
Last Verified: January 2018

Additional relevant MeSH terms:
Carcinoma, Non-Small-Cell Lung
Carcinoma, Bronchogenic
Bronchial Neoplasms
Lung Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Neoplasms
Lung Diseases
Respiratory Tract Diseases
Levonorgestrel
Ethinyl estradiol, levonorgestrel drug combination
Ethinyl Estradiol-Norgestrel Combination
Nintedanib
Ethinyl Estradiol
Contraceptive Agents, Female
Contraceptive Agents
Reproductive Control Agents
Physiological Effects of Drugs
Contraceptives, Oral, Synthetic
Contraceptives, Oral
Antineoplastic Agents
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Estrogens
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Contraceptives, Oral, Combined
Contraceptives, Postcoital, Synthetic
Contraceptives, Postcoital