Orgovyx (relugolix) vs Akeega (niraparib and abiraterone acetate)

Orgovyx (relugolix) vs Akeega (niraparib and abiraterone acetate)

Orgovyx (relugolix) is an oral gonadotropin-releasing hormone (GnRH) receptor antagonist used primarily for the treatment of advanced prostate cancer by reducing testosterone levels, which can slow the growth of prostate cancer cells. Akeega (niraparib and abiraterone acetate) combines a PARP inhibitor (niraparib) and a CYP17 inhibitor (abiraterone acetate), and is used for treating metastatic castration-resistant prostate cancer (mCRPC), often in patients with specific genetic mutations or after other hormone therapies have failed. When deciding between Orgovyx and Akeega, patients should consider factors such as the specific stage and genetic characteristics of their prostate cancer, previous treatments, potential side effects, and the mode of administration, as Orgovyx is a single agent oral medication while Akeega combines two medications with potentially different side effect profiles.

Difference between Orgovyx and Akeega

Metric Orgovyx (relugolix) Akeega (niraparib and abiraterone acetate)
Generic name Relugolix Niraparib and Abiraterone Acetate
Indications Advanced prostate cancer Prostate cancer
Mechanism of action GnRH receptor antagonist Poly (ADP-ribose) polymerase inhibitor and androgen biosynthesis inhibitor
Brand names Orgovyx Akeega
Administrative route Oral Oral
Side effects Hot flushes, increased glucose, musculoskeletal pain, fatigue, diarrhea, and increased triglycerides Hypertension, hypokalemia, edema, increased liver enzymes, fatigue, and arthralgia
Contraindications Patients with known hypersensitivity to relugolix or any components of the product Patients with known hypersensitivity to niraparib, abiraterone acetate, or any excipients in the formulation
Drug class Gonadotropin-releasing hormone (GnRH) antagonist Poly (ADP-ribose) polymerase (PARP) inhibitor and CYP17 inhibitor
Manufacturer Myovant Sciences Janssen Biotech, Inc.

Efficacy

Orgovyx (Relugolix) Efficacy in Prostate Cancer Treatment

Orgovyx (relugolix) is an oral gonadotropin-releasing hormone (GnRH) receptor antagonist indicated for the treatment of adult patients with advanced prostate cancer. Clinical trials have demonstrated the efficacy of Orgovyx in rapidly reducing and maintaining low testosterone levels, which is a key therapeutic goal in the management of advanced prostate cancer. In a pivotal phase 3 study, known as the HERO trial, relugolix achieved castration levels of testosterone in 96.7% of patients, which was superior to the comparator, leuprolide, a commonly used androgen deprivation therapy (ADT).

The HERO trial also showed that relugolix had a rapid onset of action, with testosterone suppression observed as early as day 4 of treatment. This is particularly beneficial for patients requiring quick hormonal control. Moreover, relugolix was associated with a 54% lower risk of major adverse cardiovascular events compared to leuprolide, making it a potentially safer option for patients with a history of cardiovascular disease. The sustained efficacy and cardiovascular safety profile of Orgovyx present it as a significant advancement in the treatment of advanced prostate cancer.

Akeega (Niraparib and Abiraterone Acetate) Efficacy in Prostate Cancer Treatment

Akeega, which combines niraparib, a poly (ADP-ribose) polymerase (PARP) inhibitor, with abiraterone acetate, a CYP17 inhibitor, is an emerging treatment option for patients with prostate cancer. While the combination is not yet approved for clinical use, early clinical trials have shown promising results. Niraparib targets cancer cells with specific genetic mutations, such as BRCA mutations, and is thought to be effective in patients with these mutations. Abiraterone acetate works by reducing androgen production, which fuels prostate cancer growth, and is already widely used in the treatment of metastatic castration-resistant prostate cancer (mCRPC).

Initial studies suggest that the combination of niraparib and abiraterone may enhance antitumor activity and delay disease progression in patients with mCRPC. The synergistic effect of both drugs could potentially offer a more effective treatment regimen by targeting multiple pathways involved in prostate cancer growth and survival. However, further clinical trials are necessary to fully understand the efficacy and safety of Akeega in the treatment of prostate cancer. As research continues, Akeega may become an important addition to the prostate cancer treatment landscape, particularly for patients with specific genetic profiles that make them suitable candidates for PARP inhibition.

Regulatory Agency Approvals

Orgovyx
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Akeega
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

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If Orgovyx or Akeega are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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