A Phase 1 interventional study of BAY2328065 and Placebo in Endometriosis, sponsored by Bayer. Completed at 1 site in Germany. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-06-01.
Sponsored by Bayer · Phase 1, Interventional, and Treatment
Researchers are looking for a different way to treat women with a condition in which tissue that normally lines the uterus grows outside the uterus. This condition is called endometriosis. Before a treatment is available to all patients, researchers study it in clinical trials to better understand its safety and what happens to it in the body.
BAY2328065 is being developed to help treat women who have endometriosis. Women with endometriosis often have very painful menstrual periods, as well as pain in the pelvic area which is not related to menstrual periods and pain during intercourse. Many women with endometriosis may also have problems becoming pregnant. The trial treatment, BAY2328065, works by blocking a certain protein that causes pain and swelling of the tissue and is thought to play a role in endometriosis.
In this trial, the researchers want to compare what happens to different medicinal forms of BAY2328065 in the body. They also want to learn if eating a meal affects what happens to BAY2328065 in the body.
This trial will include about 32 men and women who are aged 18 to 55. There will be 4 groups of participants in this trial. The participants in Groups 1, 2, and 3 will be men. The participants in Group 4 will be women. There will be 3 treatment courses to the trial for Groups 1, 2 and 3 and 1 treatment course for Group 4.
During the trial, the participants in Groups 1, 2, and 3 will stay at the trial site for 15 days (3 times 5 days with times in between during which they stay at home). The participants in Group 4 will stay at the trial site for 16 days continuously. But, the trial will last about 6 weeks for the participants in Groups 1, 2, and 3. The trial will last about 9 weeks for the participants in Group 4.
All of the participants in Groups 1 and 2 will take the different medicinal forms of BAY2328065, with and without food. All of the participants in Groups 1 and 2 will take dose "2" of BAY2328065 in all 3 treatment courses. In Group 1, they will take BAY2328065 one time each during the following treatment courses:
The participants in Group 3 will take 3 different doses of BAY2328065 with food in each treatment course. They will take one time each during the following treatment courses:
The participants in Group 4 will either take dose "3" or "2" of BAY2328065 based on the results of treatment course 3, or a placebo. A placebo looks like a treatment but does not have any medicine in it. All of the participants will take either:
The doctors/ healthcare staff will:
The participants will:
901 studies on the registry are indexed under Endometriosis; 259 are open to participants now.
This study's enrollment of 31 is below the median of 64 across 525 interventional studies indexed under Endometriosis.
Browse Endometriosis studies →Bayer is the lead sponsor of 1,643 studies on the registry; 57 are open to participants now.
Of its 209 completed or terminated interventional studies of FDA-regulated products, 129 (62%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Approximately 6 participants will be randomly assigned to one of the 2 study intervention sequences (Group 1 or Group 2).
Drug: BAY2328065
Approximately 6 participants will be randomly assigned to one of the 2 study intervention sequences (Group 1 or Group 2).
Drug: BAY2328065
Approximately 8 participants will be assigned to the study intervention with one fixed sequence.
Drug: BAY2328065
Approximately 9 participants will be randomly assigned to receive BAY2328065.
Drug: BAY2328065
Approximately 3 participants will be randomly assigned to receive placebo.
Drug: Placebo
Solid Form, Oral administration.
Matching placebo of BAY2328065.
Number of subjects with treatment-emergent adverse events (TEAE)
Time frame: From first administration of study intervention up to 30 days after end of treatment with study intervention
Severity of treatment-emergent adverse events (TEAEs)
Time frame: From first administration of study intervention up to 30 days after end of treatment with study intervention
AUC of BAY2328065
AUC: area under the concentration vs. time curve from zero to infinity after single (first) dose
Time frame: From dosing up to 72 hours
Cmax of BAY2328065
Cmax: maximum observed drug concentration in measured matrix after single dose administration
Time frame: From dosing up to 72 hours
Plan to share: No — Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014. Interested researchers can use www.clinicalstudydatarequest.com to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the Study sponsors section of the portal.
No publications or documents are linked to this record.
This study is completed, as verified in May 2022. You cannot join it, but the record below documents what was studied.
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