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nevirapine (nevirapine ER / nevirapine XR / nevirapine, XR)

✓ Approved

Boehringer Ingelheim International GmbH · · Small Molecule

What is nevirapine?

nevirapine is a small molecule developed by Boehringer Ingelheim International GmbH. It is approved for therapeutic indications via oral (po).

Drug Profile

Brand Namesnevirapine ER, nevirapine XR, nevirapine, XR
CompanyBoehringer Ingelheim International GmbH
Drug ClassSmall Molecule
RouteOral (PO)
StatusApproved

Mechanism of Action

Molecular Targets

nevirapine acts on 1 molecular target:

gag-pol, HIV-1 (gag-pol)
Want deeper analysis?Noah AI can explain complex mechanisms and compare to similar drugs.

Therapeutic Indications

nevirapine is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Infections and infestationsAcquired immunodeficiency syndrome✓ Approved

Related Research Articles

PubMedJournal of veterinary internal medicine2026-11-12

Prolonged wireless measurement of intragastric pH and pharmacodynamics of extended-release injectable omeprazole in horses.

Hodgson Evelyn E, Thirouin Marthe M, Romano Tallia-Rume TR, Stewart Allison A et al.

Adaptation of wireless capsules for intragastric pH measurement in horses has a short, variable attachment duration. Prolonged measurement is important for pharmacodynamic studies. Extended-release injectable omeprazole (ERIO) induces acid suppression for ≤ 7 days. Five-day dosing intervals are now recommended for improved healing rates. To (1) optimize the methodology to achieve 5-7 days of capsule attachment; (2) determine whether capsules can detect a treatment effect of ERIO; and (3) describe the pharmacodynamics of ERIO. Twelve healthy adult horses. Capsules were attached transendoscopically to the glandular mucosa on day 0 using either 1 hemostasis clip (1HEM; n = 4), 4 hemostasis clips (4HEM; n = 5), or a helix tacking device (TACK; n = 9). Intragastric pH was continuously recorded and ERIO was administered on day 1. Data are reported as median (IQR). Capsules remained attached and obtained data for 51 h (42-65), 129 h (105-256), and 95 h (71-154) for 1HEM, 4HEM, and TACK, respectively. The percentage of time the pH was above 4 (%tpH > 4) was significantly higher (P < .001) on day 1 (82.0% [72.7-91.2]) than day 0 (14.3% [7.1-23.5]). Complete recordings were available for 6/12 horses throughout the 5-day dosing interval; %tpH > 4 exceeded 66% for 5 days after ERIO in 4/6 horses (66.7%). These refined, minimally invasive attachment techniques enabled longer, more consistent intragastric pH measurement. A treatment effect associated with ERIO administration was detected and %tpH > 4 exceeded 66% throughout the 5-day dosing interval in most horses.

PubMedJournal of the College of Physicians and Surgeons--Pakistan : JCPSP2026-11-12

Extended-Dose Letrozole Regimen versus Standard-Dose Regimen for Ovulation Induction and Biochemical Pregnancy in Polycystic Ovary Syndrome.

Munir Shamila Ijaz SI, Tariq Rizwana R, Raana Gule G, Butt Samia S et al.

To compare the extended-dose letrozole regimen with the standard-dose regimen for ovulation induction and biochemical pregnancy in women with polycystic ovary syndrome (PCOS). A randomised controlled trial. Place and Duration of the Study: Department of Obstetrics and Gynaecology, Sir Gangaram Hospital, Lahore, Pakistan, from April to September 2025. A total of 174 women with PCOS were randomised into extended-dose (n = 87; letrozole 5 mg, cycle days 2-10) and standard- dose (n = 87; letrozole 5 mg, cycle days 2-6) groups. Ovulation was triggered with human chorionic gonadotropin (5000 IU) upon detecting mature follicles (18-22 mm). Ovulation induction was confirmed by measuring mid-luteal serum progesterone levels on day 21, and biochemical pregnancy by urine pregnancy test on day 28. Statistical analysis was performed using both univariable and multivariable logistic regression frameworks to estimate odds ratios with 95% confidence intervals. Baseline demographics and endocrine parameters were comparable, with no statistically significant differences between groups (all p >0.05). The extended-dose letrozole regimen achieved significantly higher rates and odds of successful ovulation induction (69.0% vs. 51.7%, p = 0.020; aOR = 1.995, p = 0.035) and positive biochemical pregnancy (33.3% vs. 16.1%, p = 0.008; aOR = 2.500, p = 0.014) than the standard protocol. Conversely, secondary subfertility independently reduced the likelihood of successful ovulation induction (aOR = 0.472, p = 0.026). None of the other evaluated covariates showed a significant association in both univariable and multivariable analyses. Extended-dose letrozole regimen demonstrated better efficacy in achieving successful ovulation induction and biochemical pregnancy compared with the standard-dose regimen. However, these findings should be interpreted with caution in light of the study's inherent limitations. Letrozole, Infertility, Ovulation induction, Polycystic ovary syndrome, Pregnancy.

PubMedJournal of health monitoring2026-11-12

Who Takes Long Daytime Naps? Results of the 'German Health Update' (GEDA 2023).

Reinmuth Janina J, Löbl Simon S, Richter Almut A, Loss Julika J et al.

In the international literature, napping has been associated with positive health outcomes; however, naps lasting at least 60 minutes are linked to adverse health impacts. Until now, representative data on the frequency and duration of naps in Germany have been lacking. Using data from the representative GEDA 2023 study (n = 7,967), this fact sheet presents the prevalence of naps and extended naps (≥ 60 minutes) for women and men, stratified by age and educational groups. Almost half of the adult population in Germany takes a nap at least once a week, a quarter of whom for 60 minutes or more. Extended naps are more prevalent among women under 45 and among less educated men compared with their higher-educated peers. The results highlight the prevalence of napping in the German population, as well as the social groups that more frequently take extended naps and may therefore face higher health risks.

PubMedJournal of anesthesia, analgesia and critical care2026-11-12

Monitoring that follows the patient: from the extended recovery room to a continuous, surgery-specific postoperative pathway.

Bignami Elena G EG, Panizzi Matteo M, Macagno Francesca F, Bellini Valentina V

PubMedExpert opinion on drug metabolism & toxicology2026-11-12

Understanding pharmacokinetics of novel prolonged release dienogest 2 mg / ethinyl-estradiol 0.02 mg oral contraceptive formulation: clinical applications.

Barretta Marta M, Versailles Jacques B E JBE, Bahamondes Luis L, Juliato Cassia T CT et al.

Combined oral contraceptives (COCs) have traditionally evolved through changes in estrogen and progestin type and dose to improve safety and tolerability. More recently, drug-delivery technology has emerged as an additional strategy to modify pharmacokinetic (PK) profiles without altering hormonal components. A structured search of MEDLINE and regulatory sources was conducted to review the PK and pharmacodynamic characteristics of a prolonged-release COC containing dienogest (DNG) 2 mg and ethinylestradiol (EE) 0.02 mg, and to explore their clinical implications. Compared with immediate-release formulations, prolonged-release DNG/EE produces delayed peak concentrations, lower plasma peak levels, and reduced intra-day hormonal fluctuations while maintaining comparable overall exposure. Clinical evidence indicates contraceptive efficacy comparable to other COCs, with improved bleeding control compared with an immediate-release formulation. Both the intrinsic endometrial effects of DNG and more stable hormonal exposure may contribute to this finding. The formulation also provides antiandrogenic effects that may benefit hirsutism and acne. The safety profile appears broadly consistent with other low-dose COCs, although the effect on thromboembolic risk remains uncertain. Prolonged-release technology adds a new dimension to contraceptive choice and may facilitate individualized COC selection. Further comparative and post-marketing studies are needed to establish its clinical advantages and long-term safety.

PubMedJournal of military, veteran and family health2026-11-12

Sex differences in early release from the military: Results from a 16-year follow-up study in Canada.

Mota Natalie N, Perera Essence E, Sommer Jordana J, Enns Murray W MW et al.

Despite the increasing participation of women in the military, there has been limited exploration of sex- and gender-specific considerations in early release scenarios. This study aims to understand the sex-specific factors associated with early release from the Canadian Armed Forces (CAF) and understand the prevalence, risk correlates, and protective factors involved using a nationally representative, 16-year follow-up survey of active duty CAF members. The 2018 CAF Members and Veterans Mental Health Follow-up Survey was a 16-year follow-up of 2,941 CAF Regular Force members who participated in the 2002 Canadian Community Health Survey-Canadian Forces Supplement. The prevalence of males and females who were released following <10 and <20 years of service was calculated. Logistic regression analyses examined baseline (2002) and interim (2002-2018) risk and protective factors of releasing with <20 years of service. Early release estimates were comparable between males (11.1%) and females (13.7%). Being racialized, serving in land and sea environments, having a higher number of dependents, having greater work stress at baseline, and avoidance coping positively predicted premature release in both sexes (OR 1.10-4.04). Younger age and a higher level of deployment-related experiences were associated with a lower likelihood of early release in both sexes (AOR 0.49-0.92). Surprisingly, trauma exposure and mental disorders were mostly not positively associated with early release. Findings have implications for increasing military retention in both sexes. These implications include continued efforts to reduce work stress and unhelpful coping.

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