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Drugs for Opioid Use Disorder

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023  (Issue 1684)
, more than in any previous year.1 Several guidelines on the management of opioid use disorder ...
Opioid use disorder is a chronic, relapsing disease with physical and psychiatric components. It is associated with economic hardship, social isolation, incarceration, increased rates of blood-borne infections such as HIV and viral hepatitis, adverse pregnancy outcomes, and increased mortality. According to the NIH, there were 80,411 deaths involving an opioid in the US in 2021, more than in any previous year. Several guidelines on the management of opioid use disorder are available; all recommend maintenance pharmacotherapy as the standard of care.
Med Lett Drugs Ther. 2023 Sep 4;65(1684):137-44   doi:10.58347/tml.2023.1684a | Show Introduction Hide Introduction

Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023  (Issue 1684)
impairment Zubsolv 5.7/1.4 mg produces systemic buprenorphine levels equivalent to those seen with 8 mg ...
View Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e144-5   doi:10.58347/tml.2023.1684b | Show Introduction Hide Introduction

Niraparib/Abiraterone Acetate (Akeega) for Prostate Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023  (Issue 1684)
mutations (16.6 vs 10.9 months).1 ADVERSE EFFECTS — The adverse effects of niraparib/abiraterone acetate ...
Akeega (Janssen), a fixed-dose combination of the oral poly(ADP-ribose) polymerase (PARP) inhibitor niraparib (Zejula) and the antiandrogen abiraterone acetate (Zytiga, and others), has been approved by the FDA for use in combination with prednisone for treatment of adults with deleterious or suspected deleterious BRCA-mutated (BRCAm) metastatic castration-resistant prostate cancer (mCRPC). Niraparib has been available since 2017 for treatment of epithelial ovarian, fallopian tube, or primary peritoneal cancer. Abiraterone acetate has been available since 2011 for treatment of CRPC...
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e146-7   doi:10.58347/tml.2023.1684c | Show Introduction Hide Introduction

In Brief: Melphalan (Hepzato) for Uveal Melanoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023  (Issue 1684)
duration of response was 14 months.1 ADVERSE EFFECTS — In the FOCUS trial, cytopenias, fatigue, nausea ...
...
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e148   doi:10.58347/tml.2023.1684d | Show Introduction Hide Introduction

Talquetamab (Talvey) for Multiple Myeloma (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023  (Issue 1684)
(MonumenTAL-1; summarized in the package insert) that included 232 patients who received ≥4 prior systemic ...
Talquetamab-tgvs (Talvey – Janssen), a bispecific GPRC5D-directed T-cell engager, has been granted accelerated approval by the FDA for treatment of relapsed or refractory multiple myeloma in adults who received ≥4 prior lines of therapy, including a proteasome inhibitor, an immunomodulatory drug, and an anti-CD38 monoclonal antibody. Accelerated approval was based on the response rate and durability of response. Talquetamab is the first bispecific GPRC5D-directed T-cell engager to be approved in the US
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e149-50   doi:10.58347/tml.2023.1684e | Show Introduction Hide Introduction

Lecanemab (Leqembi) Granted Full Approval for Early Alzheimer's Disease

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
-approval for the same indication.1-3 from baseline at 18 months in the CDR-SB score was +1 ...
Lecanemab-irmb (Leqembi – Eisai/Biogen), the IV amyloid-directed monoclonal antibody that received accelerated approval from the FDA in January 2023 for treatment of early Alzheimer's disease, has now received full approval from the FDA based on a trial showing that it slowed cognitive and functional decline in patients with mild cognitive impairment (MCI) or mild Alzheimer's disease dementia and confirmed presence of brain amyloid. The IV amyloid-directed monoclonal antibody aducanumab (Aduhelm) has received only an accelerated FDA-approval for the same indication.
Med Lett Drugs Ther. 2023 Aug 21;65(1683):129-30   doi:10.58347/tml.2023.1683a | Show Introduction Hide Introduction

Bexagliflozin (Brenzavvy) — A Fifth SGLT2 Inhibitor for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
in the US for this indication (see Table 4).1 SGLT2 INHIBITORS — SGLT2 inhibitors decrease renal glucose reabsorption ...
Bexagliflozin (Brenzavvy – TheracosBio), a sodium-glucose cotransporter 2 (SGLT2) inhibitor, has been approved by the FDA to improve glycemic control in adults with type 2 diabetes. It is the fifth SGLT2 inhibitor to be approved in the US for this indication (see Table 4).
Med Lett Drugs Ther. 2023 Aug 21;65(1683):130-2   doi:10.58347/tml.2023.1683b | Show Introduction Hide Introduction

Once-Weekly or Once-Monthly Subcutaneous Buprenorphine (Brixadi) for Opioid Use Disorder

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
monthly, was the first.1 Buprenorphine is also available for treatment of opioid use disorder ...
The FDA has approved a subcutaneously injected, extended-release formulation of the mu-opioid receptor partial agonist and kappa-opioid receptor antagonist buprenorphine (Brixadi – Braeburn) for once-weekly or once-monthly treatment of moderate to severe opioid use disorder. Brixadi is the second subcutaneously injected buprenorphine formulation to be approved in the US; Sublocade, which is administered once monthly, was the first. Buprenorphine is also available for treatment of opioid use disorder in sublingual formulations with and without the opioid antagonist...
Med Lett Drugs Ther. 2023 Aug 21;65(1683):133-5   doi:10.58347/tml.2023.1683c | Show Introduction Hide Introduction

Linaclotide (Linzess) for Functional Constipation

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
idiopathic constipation and irritable bowel syndrome with constipation in adults.1 The drug has now ...
The guanylate cyclase-C receptor agonist linaclotide (Linzess – Abbvie/Ironwood) was first approved by the FDA in 2012 for treatment of chronic idiopathic constipation and irritable bowel syndrome with constipation in adults. The drug has now been approved for treatment of functional constipation in patients 6-17 years old. Linaclotide is the only drug to be approved in the US for treatment of functional constipation.
Med Lett Drugs Ther. 2023 Aug 21;65(1683):135-6   doi:10.58347/tml.2023.1683d | Show Introduction Hide Introduction

Empagliflozin (Jardiance) for Type 2 Diabetes in Children (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
has been available since 2000 for this indication. The injectable glucagon-like peptide-1 (GLP-1) receptor agonists ...
The sodium-glucose cotransporter 2 (SGLT2) inhibitor empagliflozin has been available for years alone (Jardiance – Boehringer Ingelheim) and in combination with metformin (Synjardy) to improve glycemic control in adults with type 2 diabetes. Both products have now been approved for use in children ≥10 years old. Empagliflozin is the second oral drug to become available in the US for treatment of type 2 diabetes in children; metformin has been available since 2000 for this indication. The injectable glucagon-like peptide-1 (GLP-1) receptor agonists liraglutide (Victoza) and...
Med Lett Drugs Ther. 2023 Aug 21;65(1683):e137   doi:10.58347/tml.2023.1683e | Show Introduction Hide Introduction