A Phase IIa Clinical Study to Assess the Efficacy and Saf... | NCT06963177

Status Module

Design Module

Interventional Study Design

Biospecimen

No data available

No data is available for this block.

Label	Type	Description	Intervention Names
GenSci048	Experimental	GenSci048 subcutaneously (SC) every 4 weeks.	Drug: GenSci048
Placebo	Placebo Comparator	Administered SC every 4 weeks.	Drug: Placebo

Name	Type	Description	Arm Group Labels	Other Names
GenSci048	Drug	Administered SC.	GenSci048
Placebo

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Change of dysmenorrhea (DYS) measured by Numeric Rating Scale (NRS)	The NRS for overall endometriosis-associated pain ranges from 0 (no pain) to 10 (severe pain). Higher scores mean a worse outcome.	baseline, week 24
Change of non-menstrual pelvic pain (NMPP) measured by Numeric Rating Scale (NRS)	The NRS for overall endometriosis-associated pain ranges from 0 (no pain) to 10 (severe pain). Higher scores mean a worse outcome.	baseline, week 24

Secondary Outcomes

Measure	Description	Time Frame
Change of DYS, NMPP, and dyspareunia (DYSP) measured by Numeric Rating Scale (NRS). The NRS for overall endometriosis-associated pain ranges from 0 (no pain) to 10 (severe pain). Higher scores mean a worse outcome.		52 weeks
Permitted rescue medication use.

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Pre-menopausal female participants, between 18 and 49 years of age, inclusive, at the time of signing informed consent.
Participants must have a diagnosis of endometriosis within 10 years before screening.
Have moderate to severe endometrial related pain.
Have at least one regular, natural menstrual cycles (ranging from 21 to 35 days (inclusive)) before and during the screening period.
Agree to switch from her usual analgesic medication to only that which is permitted in the study from the screening period to the end of treatment and agree to stop using other treatments for endometriosis.
Agree to use non-hormonal contraception from the time of signing the informed consent until 4 weeks after the last dose of the study medication.

Exclusion Criteria:

Participants who have previously received hysterectomy and/or bilateral oophorectomy, or plan to undergo these procedures during the study period.
Participants who suffer from chronic pelvic and/or non-pelvic pain that is not caused by EM and require chronic analgesia or other chronic treatment, which is expected to affect the assessment of EAP.
Pelvic ultrasound screening indicating a need for surgery or suspicion of malignancy.
Participants with abnormal and undiagnosed vaginal and/or uterine bleeding within 3 months prior to screening.
Participants who plan to schedule elective surgery during the study; or those who have had a surgery within 4 months prior to screening and need ongoing pain management.
History of severe depression or post-traumatic stress disorder within the two years prior to screening, or history of any other severe mental disorder at any time.
History of drug or alcohol abuse within the six months prior to screening.
Participants who have participated in any other interventional clinical trial (including clinical trials of drugs and devices) within 1 month prior to screening.
Have used a prohibited long-acting anesthetic or immediate-release anesthetic for more than 2 consecutive weeks for the treatment of endometriosis associated pain in the 6 months prior to screening.
Participant is pregnant, breast feeding, or planning a pregnancy.