Elagolix in the treatment of heavy menstrual bleeding associated with uterine fibroids in premenopausal women

Alternative therapies have developed proposing women other options for symptomatic control (pharmacological treatment) rather than a definite cure with a side damage (surgical intervention). Many of these innovative therapies exploit UF dependence on ovarian hormones. Medical therapy aims either as a short term goal to temporarily relieve women for symptoms until their surgical intervention is sought as or as long term one until there is a natural regression of UF after menopause [ 81 ]. Unfortunately, traditional hormonal medical therapies carry intrinsic risks of their own and often fail in long-term control symptoms [ 82 ]. Classically, combined oral contraceptive pills (COCs) was an attracting option for gynecologists to control UF related bleeding, considering their low cost and relatively good safety profile [ 83 ]. However, COCs showed limited efficacy especially in tumor shrinkage outcome[ 83 ]. Also, FDA approved the use of levonorgestrel-releasing intrauterine system in 2009 to treat women with HMB. However, studies have shown conflicting results on its efficacy in controlling UF related bleeding [ 84 – 87 ]. Similarly, GnRH agonist LA was one of the first used medical anti-UF treatment. In 1999, FDA approved its utility as a preoperative short-term additive in women with symptomatic UF for anemia improvement due to HMB [ 4 , 83 , 88 , 89 ]. However, acting as agonist is accompanied with delayed onset of action as well as worsening the UF related symptoms due to the initial estrogen flare effect. Additionally, its prolonged hypoestrogenism effect resulted in higher risk of BMD loss. Fortunately, this BMD changes are reversible only if treatment course is limited to 6 months. Nonetheless, continued therapy resulted in progressive and irreversible BMD loss [ 90 ]. In addition, classic menopausal side-effects such as hot flashes, vaginal dryness, and headaches limit the treatment to 6 months as well without add-back therapy [ 91 ]. Selective progesterone receptor modulators (SPRMs) have been studied extensively in the last few years with initial promising effects in induction of amenorrhea and shrinking tumor size [ 16 ]. SPRMs are synthetic ligands targeting the progesterone receptor (PR) with mixed agonist and antagonist activities [ 92 ]. Their indication as emergency contraception, termination of pregnancy, premenstrual syndrome and assisted reproduction are due their tissue-selective effects [ 93 ]. Moreover, expression of PR in endometrial and fibroid cells encouraged SPRMs investigations against UF, AUB, dysmenorrhea and endometriosis [ 82 ]. SPRMs family includes Mifepristone, Asoprisnil, Onapristone, ulipristal acetate (UPA), Lonaprisan, Vilaprisan and Telapristone. Notably, enthusiasm about SPRMs was attributed to their minimal effect on serum estrogen levels therefore they are not expected to induce menopausal-like symptoms or subsequent bone loss [ 92 – 95 ]. Vilaprisan dosed in 1–5 mg daily for 12 week induced profound bleeding cessation in women with UFs which supported further advancement of clinical trials to evaluate vilaprisan in women with symptomatic UFs [ 96 ]. However, long-term toxicological animal studies using high doses revealed safety concerns, therefore all current trials were paused [ 97 ]. A main known risk with the use of SPRMs is their association with a reversible morphological change in the endometrial lining known as progesterone-receptor modulator-associated endometrial changes (PAECs) after prolonged exposure [ 82 , 98 ]. UPA was approved and prescribed in Europe, Canada and Australia for few years but recent studies found that UPA could cause liver failure that may require liver transplantation [ 17 , 18 ] and EMA called for temporary suspension of UPA (Esmya™) and generic medicines sales. Off note, The EMA’s review is restricted only to UPA 5mg for the treatment of UFs and does not affect its use in 30mg as a single-dose medicine (ellaOne) for EC, as there is currently no concern about liver injury with the latter [ 99 ]. The utility of new-generation oral GnRH-antagonists, such as elagolix, relugolix and linzagolix is offering a new potential opportunity for the future therapy of UFs: elagolix has been the most studied drug of this class for treating benign gynecological diseases including endometriosis and UFs, for which it has been approved in 2018 and 2020 respectively [ 100 , 101 ]. Notably, elagolix is the only and first FDA approved oral treatment for UF associated bleeding with advantage over the injectable antagonists that it offers less frequent regimen and better safety profile. Studies explored different dosage regimens of elagolix to balance the efficacy and safety and concluded 300 mg twice daily in combination with add back therapy to fit the best based on Phase III ELARIS studies as well as population-based PK studies. Further studies will identify best population to benefit from the therapy in addition to long term safety profile. Interestingly, upon drug discontinuation, hormonal level was found to return rapidly to normal values along with restoration of menstruation which represent an advantage for women pursuing future fertility [ 102 ]. Recently, a case report was published showing a debulking effect of elagolix on a uterine adenomyoma [ 103 ]. Other GnRH-antagonist, relugolix is recently licensed in Japan for UF related symptoms management following several Phase III clinical trials showing it efficacy in UF associated pain [ 102 , 104 ]. In United States, extensive phase III studies are currently exploring its efficacy in UF and prostate cancer. For prostate cancer, relugolix, as oral androgen deprivation therapy, achieved rapid, sustained suppression of testosterone levels that was superior to that with leuprolide, with a 54% lower risk of major adverse cardiovascular events [ 105 ]. For UF, ongoing phase III 24 week trials (Liberty 1 and 2) are conducted in women with UF associated HMB exploring combination therapy of relugolix 40 mg, E2 1 mg, NETA 0.5 mg, or delayed relugolix combination therapy (relugolix 40 mg monotherapy followed by relugolix combination therapy, each for 12 weeks) compared to placebo control (LIBERTY 1, NCT03049735 ; LIBERTY 2, NCT03103087 ). Of note, relugolix has longer t 1/2 that allows for once daily administration and may improve patients’ compliance in long-term therapy [ 106 ]. The recent explored GnRH antagonist is linzagolix (OBE2109), alone and in combination with add-back therapy in 2 ongoing prospective, randomized, parallel-group, double-blind, placebo-controlled phase III studies for treatment of UF associated HMB in premenopausal women( NCT03070951 and NCT03070899 ).

Elagolix has molecular formula of C 32 H 30 F 5 N 3 O 5 and molecular weight of 631.6 g/mol. Elagolix sodium is a non-peptide, amorphous solid orally bioavailable small molecule, that is freely soluble in water. Elagolix at 150 or 200 mg dose, is highly soluble throughout the physiological pH range, and exhibits high aqueous solubility (approximately 1 mg/mL) as per the biopharmaceutics classification system (BCS) [ 22 ]. Chemical structure of elagolix is shown in figure 1 . Studies showed that elagolix is rapidly absorbed with a time to maximum concentration (T max ) of approximately 1 hour, while the maximum concentration [C max ] and area under the curve [AUC]) are dose proportional from 100 to 400 mg twice daily dose, and more than dose proportional with single doses of 600–1200 mg based on clinical pharmacokinetics studies in healthy subjects [ 23 ]. An absorption study was conducted in 6 healthy subjects to examine elagolix 100 mg pharmacokinetics (PK) administered to the stomach via oral solution, and to the jejunum, ileum, and colon via a radiolabeled remote drug delivery capsule. Briefly, both routes resulted in comparable overall systemic exposure, except for the colon administration which represented less than 10% that of the same dose deposited into the stomach/duodenum, jejunum, or ileum [ 24 ]. Data derived from 1624 subjects involved in five phase I and four phase III studies were employed in population PK analyses, with results showing that none of the tested covariates were significantly associated with Elagolix PK parameters, including age, body weight, race/ethnicity, hepatic or renal function, except for hepatic uptake transporter OATP1B1 genotype status which was significant (i.e. specifically for CL/F) [ 25 ]. The effect of food on elagolix plasma exposure was assessed via administration of a high-fat meal with result observed of a slight reduction relative to the fasted condition. Consequently, Elagolix was administrated at least 1 h before or 2 h after a meal in attempt to avoid a potential lower exposure in three of four endometriosis phase III pivotal clinical trials. Interestingly, elagolix was administered without regard to meals in the fourth endometriosis phase III extension trial and the clinical efficacy results were similar, regardless of drug administration instructions with respect to meals. Therefore, elagolix can be administered with or without food [ 24 ]. About 80% of elagolix is bound to human plasma proteins, with blood-to-plasma ratios of 0.6 as drug found to preferentially partitioned into plasma rather than blood cellular components [ 26 ]. Population PK data showed that elagolix estimated apparent central volume of distribution ( V c/ F ) was 257 L[ 24 ]. In vitro studies in addition to pharmacogenetics analysis showed that elagolix is a substrate of hepatic uptake transporter OATP1B1. However, population PK analysis did not identify the OATP1B1 genotype as a significant covariate on elagolix V c/ F [ 25 ]. In vitro studies showed that elagolix is metabolized by multiple cytochrome P450 (CYP450) enzymes with major contribution from CYP3A4 (approximately 50%), and minor contributions from other CYP450s [ 24 ]. Following the administration of a single oral dose of 150 mg of radiolabeled [ 14 C] elagolix to 6 healthy subjects, about 69% of elagolix was recovered in feces and urine as metabolites. These data suggest that unchanged elagolix is the major drug-derived material in human plasma and elagolix is extensively metabolized [ 24 ]. After reaching C max, elagolix concentration–time profile exhibits biphasic characteristic, with an apparent terminal elimination half-life ( t 1/2 ) of approximately 4–6 hrs. Therefore, repeated dosing of elagolix once or twice per day does not result in significant drug accumulation in plasma [ 23 , 25 ]. Elagolix dose adjustment is not required in women with any degree of renal impairment or end stage renal disease (including women receiving dialysis). While in women with severe hepatic impairment (Child–Pugh C), elagolix C max and AUC were increased by 520% and 570%, respectively. Therefore, elagolix is contraindicated in women with severe hepatic impairment (Child–Pugh C) [ 27 ]. Table 1 summarizes pharmacokinetics parameters for elagolix in healthy volunteers. Elagolix has a dose-dependent suppression effect on the gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH) which subsequently decreased blood concentrations of the ovarian sex hormones estrogen (E2) and progesterone [ 20 , 23 , 28 ]. Elagolix induced a dose-dependent suppression of sex hormones in premenopausal females when consumed in regimens; 150 mg once daily, or 100, 200, 300, or 400 mg twice daily for 21 days as compared to placebo. Interestingly, it took only hours following first dose administration of the on day 1 to achieve that effect which continued through day 21. Notably, maximum E2 suppression was achieved with regimen starting from 200 mg elagolix twice daily or higher. Interestingly, LH suppression was more noticeable than FSH in all groups except for the 150 mg once daily group. Upon elagolix discontinuation, LH and FSH levels rose within 24 h after the last dose, and E2 levels began to rise 24 h after the last dose was administered [ 24 , 29 ]. The effects elagolix in different doses and dosing regimens either alone or in combination with standard dose hormonal add-back therapy (E2/norethindrone acetate (NETA) 1 mg/0.5 mg) on ovulation, ovarian activity, and ovarian reserve were evaluated in a study in healthy adult premenopausal females for 3 month with similar finding of dose dependent hormonal suppression [ 27 , 30 ]. Studies showed that the standard dose of E2/NETA as 1 mg/0.5 mg, when administered exogenously with elagolix, provided the optimal plasma levels of E2 which was similar among endometriosis patients as well as healthy subjects [ 24 , 26 , 31 ]. Following pivotal phase III ELARIS studies on premenopausal women moderate-to-severe pain associated with endometriosis, recent study explored the relationships between elagolix exposures and clinical efficacy response rates for dysmenorrhea and non-menstrual pelvic pain [ 32 ]. This study employed nonlinear mixed-effects discrete-time first order Markov modeling approach to characterize the relationships between elagolix average concentrations and efficacy responses. Results suggested no preference of one regimen over the other to treat endometriosis-associated pain for any patient subpopulation based on tested covariate groups. Several studies explored potential drug-drug interactions of elagolix with other drugs such as Ketoconazole, rosuvastatin, digoxin, midazolam, sertraline, fluconazole and rifampin in terms of change in elagolix C max and AUC with conclusion of concomitant use of strong inhibitors of OATP1B1 is contraindicated with elagolix [ 33 – 35 ]. To account quantitatively for the contribution of metabolizing enzymes, transporters, and their interplay in Elagolix PK, a whole-body physiologically based pharmacokinetic (PBPK) model of Elagolix was developed which adequately recovered the observed drug–drug interaction [ 34 ]. Importantly, results showed that combinations of elagolix with norethindrone or triphasic oral contraceptives (OCs) did not negatively impact the hormonal effects of each other, consequently no dose adjustment is required. [ 36 ]. Phase I clinical studies regarding Elagolix showed that, 5 of 9 cohorts in phase I clinical study received a single dose of elagolix 25 mg, 50 mg, 100 mg, 200 mg, 400 mg, or placebo [ 29 ]. The first dose of elagolix was administered on day 7 + 1 after menstruation onset. Suppression of LH and FSH was achieved in all groups, whereas a dose dependent suppression of LH, FSH and E2 was noted [ 29 ]. In another phase I clinical study regarding to hormone response, safety, and PK, elagolix 150 mg once daily, as well as elagolix 100 mg, 200 mg, 300 mg, and 400 mg twice daily were compared to a placebo. Treatment intake was started two days after the onset of menstruation. The results were similar to previous studies: A dose-dependent suppression of E2, progesterone, LH, and FSH was observed, the suppression of FSH being the most efficient with elagolix 300 mg and 400 mg, while the clearest decrease in LH and E2 was found with elagolix 200 mg. The concentration of progesterone remained at anovulatory levels throughout the study period at the lowest dose of elagolix [ 23 , 37 ] Starting from Phase II trials, elagolix was investigated in patients with endometriosis and UFs. The first stage of one Phase II study lasted 12 weeks and compared 3 groups with one another: a placebo control group; a group of patients receiving 150 mg elagolix once daily; and a third group receiving 250 mg once daily. Endometriosis-associated pain had decreased in all three groups by the end of the 12 weeks, as assessed by the Numeric Rating Scale. After 12 weeks, the patients of the placebo group were reallocated to one of the groups receiving elagolix. In this second stage, there was a further reduction of dysmenorrhea in both groups. Similar results were achieved for dyspareunia. Statistical significance was seen between elagolix 150 mg and placebo during weeks 8 to 12, as well as between elagolix 250 mg and placebo during weeks 4 to 8. Furthermore, a decrease in the use of prescription analgesics was seen in the elagolix groups, while the biggest improvement in quality of life was noted specifically in the elagolix 150mg group [ 38 ]. Similar results were described in another phase II clinical trial conducted showing the effect of 150 mg elagolix compared to placebo over an eight-week, double-blind, placebo- controlled treatment period, followed by a 16-week open-label treatment period [ 39 ]. Consequently, in May 2017, the results from two multicenter, double blind, randomized, placebo-controlled, phase III trials (Elaris EM-I and Elaris EM-II) were published. The patients enrolled in both studies were premenopausal women who had surgically diagnosed endometriosis and suffered from moderate to severe endometriosis-associated pain. 653 (74.9%) out of 871 women included in EM-I, completed the six-month study period. In the nearly identical EM-II,815 were women treated, with 632 (77.4%) completing the trial. The patients who completed the trials were enrolled in either a 6-month extension study (EM-III or EM-IV) or included in the 12-month follow-up period. The primary endpoints of the placebo-controlled EM-I and EM-II were efficacy, with regard to alleviation of dysmenorrhea and non-menstrual pelvic pain (NMPP), after three months of elagolix 150 mg once daily or Elagolix 200 mg twice daily, compared to placebo, measured in a reduced pain and reduced or equivalent intake of rescue analgesics. After three months of treatment in the EM-1, 46.4% of the women treated with elagolix 150 mg once daily,, and 75.8% of the patients treated with elagolix 200 mg twice daily, vs 19.6% of the women in the placebo group, were noted to be dysmenorrhea responders, which refers to participants who had a clinically meaningful reduction in the pain score and a decreased or stable use of rescue analgesic agents, as recorded in a daily electronic diary, while 50.4% of the women treated with elagolix 150 mg once daily and 54.5% of the women treated with 200 mg elagolix twice daily vs 36.5% of the women in the placebo group, were described as ‘non-menstrual pelvic pain responders.’ Similar results were found in the EM-II for the 150 mg once daily group, the 200 mg twice daily group, and the placebo group, with 43.4% and 72.4% vs 22.7%, respectively, of women who described a reduction of dysmenorrhea and 49.8% and 57.8% vs 36.5%, respectively, of women who described a reduction of non-menstrual pelvic pain, as well as a decrease or the same in intake of analgesics. After three and six months, the difference in intake of rescue analgesics between the elagolix 150 mg group and the placebo group was not found to be significant, while the contrary was noted in the group of women who received the higher dose compared to the placebo. Furthermore, a significant improvement in quality of life was noted in the elagolix-treated groups, as determined by 30-item Endometriosis Health Profile Scores [ 40 ]. A randomized, double-blind, multicenter, placebo-controlled phase III trial showed that elagolix significantly reduces fatigue levels in women with moderate or severe endometriosis-associated pain [ 41 ]. Moreover, another study employed post hoc analysis of pooled data from the phase III ELARIS-I and ELARIS-II clinical trials to the relationship of clinically meaningful improvements in dyspareunia with health-related quality of life changes among women with endometriosis [ 42 ]. Several articles in the literature covered in details utility of elagolix for endometriosis associated pain over the past few years for further reading [ 43 – 66 ]. Two multicenter phase II studies evaluated elagolix in premenopausal women with UFs for its efficacy in controlling bleeding. In both trials, either elagolix monotherapy or in combination with hormonal add-back therapy (E2 and NETA) was evaluated and the primary endpoints in the Phase IIa study was mean change in MBL from baseline to the last complete menstrual cycle (last 28 days) during treatment and in the phase IIb study the primary endpoint was the percentage of women with MBL volume of less than 80 mL and of more than at least 50% reduction in MBL volume at the end of the study during last 28 days of treatment using accurate alkaline hematin method [ 30 , 31 ]. In the phase IIa trial, seven dosing regimens of elagolix were explored including twice daily of 100 mg, 200 mg or 300 mg or once daily of 400 mg or 600 mg, or twice daily of 200 mg combined with continuous E2 0.5 mg/NETA 0.1 mg or twice daily 300 mg combined with both continuous E2 1 mg and cyclical progesterone 200 mg only for 12 days monthly, in attempt to find minimally efficacious elagolix doses with a lower frequency of administration. In the elagolix group, a significantly dose dependent reduction in MBL was observed (with highest reduction in patients receiving the drug at 300 mg BID) compared to the placebo group as well as significant decrease in largest UF volume among treated groups [ 30 ]. In the phase IIb trial, women were randomized into two cohorts, cohort 1 included 259 patients received 300 mg twice daily and cohort 2 included 308 women received 600 mg once daily. Each cohort was randomized into 4 groups including placebo, elagolix alone and elagolix with add-back therapy either low dose of E2 0.5 mg/NETA 0.1 mg or high dose of E2 1 mg/NETA 0.5 mg [ 31 ]. At the end of the study, primary endpoint criteria were met in 92% in elagolix alone groups of 300 mg BID and 90% in 600 mg QD, adding low dose add-back therapy reduced the percentage to 85% and 73% while high dose add-back therapy resulted in 79% and 82% in aforementioned groups, respectively (p < 0.001, each treatment group compared to placebo). Moreover, all treated groups showed significant UF tumor shrinkage at final visit from baseline, with the exception in 600 mg daily with 1.0 mg estradiol/0.5 mg norethindrone acetate. Finally, improvement in the symptom severity was observed in all patients in treatment groups [ 31 ]. Phase III trials, Elaris UF-I and Elaris UF-II were published early 2020 evaluating the safety, tolerability, and efficacy of 6-month Elagolix treatment in women with UFs. Tested dosage regimens were twice daily of 300 mg elagolix either alone or in combination with hormonal add-back therapy (E2 1 mg / NETA 0.5 mg). Elagolix-alone group was included to evaluate the add-back therapy effect on the hypoestrogenic effects of elagolix. Same as phase II trials, the primary endpoint was the percentage of women with MBL less than 80 mL at final month and at least 50% MBL reduction at final month from baseline [ 67 ]. Elagolix plus add-back therapy resulted in meeting criteria for the primary end point in 68.5% of 206 women in UF-1 and in 76.5% of 189 women in UF-2, while in placebo group only 8.7% of 102 women and 10% of 94 women only reported improvement (P<0.001). As expected, elagolix alone has better outcome in 84.1% of 104 women in UF-1 and in 77% of 95 women in UF-2. Nevertheless, add-back therapy attenuated elagolix hypoestrogenic effects especially BMD loss, while hot flushes (in both trials) and metrorrhagia (in UF-1) occurred significantly more commonly compared to placebo. Later, ELARIS UF EXTEND study was published as phase III multicenter, randomized, double-blind, extension study [ 68 ]. Where an additional 6 months (up to 12 months total) of elagolix 300 mg twice daily with hormonal add-back therapy (E2 1 mg and NETA 0.5 mg once daily) in women who completed an initial 6 months of the same treatment in one of two preceding phase 3 ELARIS UF-1 and UF-2 studies to evaluate the long-term efficacy, tolerability, and safety and, in particular, to characterize the impact of add-back on the hypoestrogenic effects of elagolix especially BMD changes and following the same endpoints of the original study. Results showed that total 12 months of combination treatment still sustained MBL reduction while no new or unexpected safety concerns were associated with an additional 6 months of treatment, also using add-back therapy attenuated the hypoestrogenic effects of elagolix alone [ 68 ]. Similarly, increasing number of articles discussing the beneficial role of elagolix in UF bleeding and increasing afflicted women quality of life are being published in literature [ 69 – 72 ]. Table 2 summarizing clinical trials conducted to explore efficacy of elagolix in UF associated bleeding. Similar adverse events were described throughout all clinical trials phases. Mild to moderate nausea and hot flashes were reported as the most common adverse events with the highest incidence of hot flashes occurred in women receiving an elagolix dose of at least 200mg twice daily. Furthermore, spotting was reported by seven patients included in this phase 1 study. However, these adverse events didn’t lead to a discontinuation of study participation. Additionally, no changes or differences from the placebo group were found with regard to electrocardiograms, blood tests, or vital signs [ 23 , 73 ]. Importantly, a phase 2 conducted study in endometriosis patients showed a significant decrease in bone-mineral density (BMD) was noted in both the elagolix 150mg and elagolix 250mg groups [ 38 ] where a significant dose-dependent decrease of lumbar BMD was noted after six months of treatment in both groups. Laboratory results from a phase 3 study showed an elagolix-associated increase in low-density and high-density lipoprotein cholesterol, as well as triglycerides [ 73 ]. A phase 1 study was conducted in healthy premenopausal females to evaluate whether elagolix has potential QTc interval prolongation with conclusion of no clinical relevance [ 24 , 74 ]. Data from four phase III studies were used in Exposure–BMD modeling where simulations of 36 months of continuous treatment suggested a mean percentage of 2% and 5% change in lumbar spine BMD from baseline for Elagolix 150 mg once daily or 200 mg twice daily respectively. This data is consistent with the observed 1% BMD change after 12 months treatment of 150 mg once-daily dosing. Collectively, these studies supported the indicated use of elagolix 150 mg once daily for 24 months or 200 mg twice daily for 6 months [ 33 , 40 , 75 – 78 ]. In Elaris UF-1 and UF-2, adverse reactions caused discontinuation rate of 10% among women treated with elagolix supplemented with add-back therapy and 7% among placebo-treated women. The most common reported adverse events leading to study drug discontinuation in the elagolix plus add-back group were nausea, headache, alopecia, metrorrhagia, menorrhagia, and hot flush (1% each) [ 75 ]. Furthermore, subset analysis of the Phase III studies was performed to evaluate the safety and efficacy of elagolix (300 mg twice a day) with add-back therapy (1 mg E2/0.5 NETA once a day) in reducing HMB associated with UFs in various subgroups of women over 6 months of treatment where subgroups analyzed included age, body mass index, race, ethnicity, baseline MBL, fibroid location, and uterine and primary fibroid volume (largest fibroid identified by ultrasound). Study concluded efficacy of elagolix with hormonal add-back therapy in reducing HMB associated with UFs independent of any of these factors [ 79 ]. Pharmacoeconomic study was conducted to assess the cost–effectiveness of Elagolix versus GnRH agonist LA in women with moderate to severe endometriosis pain using a Markov model with a positive net monetary benefit (NMB) in favor of Elagolix over LA over 1- and 2-year time horizons [ 80 ]. Elagolix was developed by AbbVie and Neurocrine Biosciences for management of hormone-dependent reproductive disorders in women. Subsequently, In July 2018, the US FDA approved elagolix tablets (ORILISSA™) for management of moderate to severe pain associated with endometriosis. In May 2020, FDA approved ORIAHNN™ (Elagolix, estradiol, and norethindrone acetate capsules; Elagolix capsules) as the first oral medication for the management of heavy menstrual bleeding due to UFs in pre-menopausal women as One capsule (elagolix 300 mg, E2 1 mg, NETA 0.5 mg) in the morning and one capsule (elagolix 300 mg) in the evening for up to 24 months [ 33 , 75 ].

Uterine Fibroids are the most common benign tumor in reproductive age women worldwide, with financial burden of hundreds of billions of dollars annually including direct cost of hospital admission and medical management as well as indirect cost of loss of wages and productivity loss. Unfortunately, there is limitation in available long-term treatment options. Thus, there is a large unmet need in the UF space for noninvasive therapeutics. Elagolix is an oral GnRH antagonist that suppresses steroidal hormones production in a dose-dependent manner. Elagolix with add-back therapy is the first oral FDA approved drug for management of UF associated HMB up to 24 months due to the risk of continued bone loss.

Uterine Fibroids (UFs) are the most common benign tumor in reproductive age women worldwide worldwide, UFs are rare before puberty (menarche), their likelihood increases as women age during their reproductive years and reach its peak before menopause then UFs typically regress following menopause, with prevalence of 70% and 80% in Caucasian and African American women respectively by age of 50 [ 1 – 3 ]. Accordingly, it has a profound impact on health care costs worldwide. In the USA alone, UFs cost range estimated between 6 and 34 billion dollars annually [ 4 ]. The mechanism underlying UFs pathogenesis remains unclear, which in turn limits its effective treatment. Growing evidences support the theory that these monoclonal tumors originate from aberrant stem cells in the myometrium and involves numerous factors such as sex steroid hormones, estrogen and progesterone, various growth factors, and genetic factors [ 5 ]. If possible, many women with UFs would choose pharmacological treatment over a surgical treatment to secure their future family plans and avoid major surgeries [ 6 , 7 ]. Several factors should be considered on individual basis when selecting appropriate UF treatment including patient’s age, symptoms severity, individual preferences and most importantly patient’s future family plans. Currently, there is limitation in available long-term medical treatment options. Thus, there is a large unmet need in the UF space for noninvasive therapeutics [ 8 , 9 ]. Therefore, extensive studies exploring mechanistic insights behind UF pathogenesis are needed for sake of developing new UFs therapeutics. Estrogen and progesterone signaling are imperative for tumor growth. Therefore, current investigated treatment options aim to halt that hormonal effect including gonadotropin releasing hormone (GnRH) antagonists and selective progesterone receptor modulators (SPRMs) [ 10 ]. Till early 2020, the only agent FDA-approved medical treatments for UFs in the USA was leuprolide acetate (LA), gonadotropin-releasing hormone (GnRH) agonist, for improvement of anemia preoperatively only for short-term (3–6 months) [ 11 ]. This effect was due to suppression of ovarian estrogen and progesterone which shrink tumor volume and reduce surgical blood loss [ 12 ], Nevertheless, the resultant bone density loss along with the recurrence of UF symptoms following treatment cessation, discouraged the utility of this drug as long term therapy for UFs [ 13 ]. Later, GnRH Antagonists utility offered an advantage over GnRH agonists which is avoiding the initial flare effect resulted from receptor stimulation (up to 15 days), so they can exert faster effect of bleeding cessation [ 14 , 15 ]. SPRMs are synthetic steroid ligands with a progesterone receptor-target and tissue-selective effects of mixed agonist and antagonist activities [ 16 ]. Ulipristal acetate (UPA) is commonly used SPRM and was approved against UFs in Europe and Canada with advantage of lacking the hypoestrogenic symptoms of GnRH analogs [ 16 ]. However, recent studies found that use of UPA is associated with the risk of liver failure that may require liver transplantation [ 17 , 18 ]. Therefore, currently SPRM use is restricted. European medicine agency (EMA) recommends UPA can now only be used to treat uterine fibroids in premenopausal women for whom surgical procedures (including uterine fibroid embolization) are not appropriate or have not worked. Also, the medicines must not be used for controlling symptoms of uterine fibroids while awaiting surgical treatment [ 19 ]. Oral GnRH antagonist are extensively studied now for the treatment of heavy menstrual bleeding associated with UFs including elagolix, relugolix and linzagolix. Elagolix is the only FDA approved for the treatment of moderate to severe pain associated with endometriosis [ 20 , 21 ] and elagolix supplemented with estradiol and norethindrone acetate was recently approved as first oral treatment for UFs associated heavy menstrual bleeding. In this drug profile we reviewed the literature of elagolix covering its chemistry, pharmacokinetics, pharmacodynamics, clinical efficacy and safety. In addition, where its stands among other therapies explored against UFs.