|Year : 2022 | Volume
| Issue : 6 | Page : 452-458
Paxlovid: A promising drug for the challenging treatment of SARS-COV-2 in the pandemic era
Niraj Niraj1, Sonia Shinde Mahajan2, Ajay Prakash1, Phulen Sarma1, Bikash Medhi1
1 Department of Pharmacology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
2 Department of Pharmacology, All India Institute of Medical Sciences, Jammu, Jammu and Kashmir, India
|Date of Submission||25-Apr-2022|
|Date of Decision||15-Jan-2023|
|Date of Acceptance||16-Jan-2023|
|Date of Web Publication||31-Jan-2023|
Department of Pharmacology, Research Block B, 4th Floor, Room No 4043, Postgraduate Institute of Medical Education and Research, Chandigarh - 160 012
Source of Support: None, Conflict of Interest: None
Coronavirus infection is a pandemic threat and the most dangerous disease of the 21st century. Despite the rigorous exertion of world-class researchers, there is no perfect cure for it. It has been seen in presently available studies that Paxlovid prevents the progression of diseases and reduces severity in patients tremendously who are at high risk of hospitalization and death. It is a safe oral antiviral drug and has the potential to treat infections from multiple corona variants including omicron which affects humans. Paxlovid is comparatively less expensive than other available effective medicines. Consequently, it reduces hospitalization and death and helps to plummet the economic burden on patients and the health-care system globally. This medicine is still under investigation, and numerous clinical trials are still underway. Its potential side effects are minor and well tolerated by research study participants. Studies show its benefits outweigh the risk, and it is an effective and good alternative for the treatment of coronavirus disease.
Keywords: Antiviral treatment, coronavirus disease, Paxlovid
|How to cite this article:|
Niraj N, Mahajan SS, Prakash A, Sarma P, Medhi B. Paxlovid: A promising drug for the challenging treatment of SARS-COV-2 in the pandemic era. Indian J Pharmacol 2022;54:452-8
|How to cite this URL:|
Niraj N, Mahajan SS, Prakash A, Sarma P, Medhi B. Paxlovid: A promising drug for the challenging treatment of SARS-COV-2 in the pandemic era. Indian J Pharmacol [serial online] 2022 [cited 2023 Sep 23];54:452-8. Available from: https://www.ijp-online.com/text.asp?2022/54/6/452/368838
| » Introduction|| |
Coronavirus infection is a pandemic threat and the most dangerous disease in the 20th century. SARS-COV-2 viruses are continuously mutating, and their nature is unpredictable. Around 400 million people are suffering, and approximately 5.7 million deaths have occurred worldwide, which is increasing in number. Due to this terrible desolation, people are suffering physically, economically, and psychologically. Despite the consummate crusade of world-class research, there is no perfect cure for this lethal disease neither in the form of therapeutic medication nor as ideal vaccines. The structure of the virus is highly complex, and its numerous mutations are progressively dilapidating human existence.
Paxlovid is a therapeutic combination of two drugs, namely, nirmatrelvir and ritonavir. It prevents the progression of the disease and reduces its severity in COVID-19 patients tremendously. However, research on it is still ongoing. It received the Emergency Use Authorization (EUA) from the U. S. Food and Drug Administration (FDA) to combat mild-to-moderate conditions for COVID-19 patients who are 12 years and/or older and carry a high risk of progression to severe disease, hospitalization, or death. Very few studies have been published in this regard, and many clinical trials as mentioned further are ongoing. In the present article, we have discussed the efficacy and safety of Paxlovid from the available published literature and summarized ongoing clinical trials.
| » Mechanism of Action|| |
Paxlovid is an antiviral preparation containing nirmatrelvir and ritonavir. It works intracellularly and inhibits the main protease (Mpro) of the SARS-CoV-2 virus. It inhibits the replication of viral RNA in the proteolytic stage. Nirmatrelvir is the Mpro inhibitor that blocks the replication of coronavirus (SARS-COV-2 Mpro), whereas ritonavir is a strong inhibitor of cytochrome P 450 (CYP) 3A which inhibits the metabolism and breakdown of nirmatrelvir so that it remains active at higher concentrations in the body for a longer duration.
Paxlovid is a safe oral antiviral drug. A study done on 1881 patients observed that Paxlovid compared with placebo had 19% and 21% adverse events, respectively. Most of the events were of mild intensity. Nearly 1.7% of serious adverse events were observed in Paxlovid-treated patients, whereas 6.6% were seen in placebo-treated ones. The study was discontinued when 2.1% of serious adverse events occurred in the Paxlovid arm and 4.1% in the placebo arm. A pivotal EPIC-HR study of Paxlovid in transplant patients suggests that it should not be given to those who are highly dependent on CYP3A4 for their clearance. Ritonavir is a strong inhibitor of the cytochrome P450 and p-glycoprotein, and hence, the dose should be monitored and individualized. Furthermore, the FDA has suggested that it is not recommended for those patients who have a history of liver or renal function impairment. However, clinicians must be vigilant and active monitoring of the patient is required during Paxlovid use. It is important to perform risk management when Paxlovid efficacy outweighs the risk to individual transplant recipients.
Paxlovid (nirmatrelvir (PF-07321332) + Ritonavir) is the first oral antiviral therapy administered for coronavirus treatment which is authorized only by the prescription in the United States of America (U. S. A). The data available regarding efficacy of paxlovid in the treatment of COVID-19 are summarized in [Table 2]. In the clinical trial, scheduled interim analysis proved that this drug reduces dramatically, i.e., by 89%, the risk of hospitalization or death in the patients suffering from COVID-19 in comparison to the placebo. Paxlovid reduces the mortality in patients within 3 days of onset of symptom, with only 0.8% (3/339) admitted to the hospital on the 28th day after randomization and occurrence of no deaths., Hospitalization of 7% (27/385) and deaths of 1.81% of patients were seen in the placebo arm. Furthermore, it had been noticed that, in those patients who were treated with Paxlovid within 5 days of symptom onset, hospitalization was seen in only 1% (6/607) of patients and no deaths were observed., However, hospitalization was seen in 6.7% (41/612) of patients and deaths in ten patients (1.6%) in the placebo arm., The results of both studies were highly significant (P < 0.0001). Furthermore, in phase 2 and 3 trials, a primary interim analysis of enrolled 1219 adult patients showed that Paxlovid reduced death and hospitalization by 89%.
In another clinical trial, 70% of the 3000 patients were from across the world (North and South America, Africa, Asia, and Europe), and out of these 3000 patients, 45% of patients were from the USA.,, The Europe Medicine Agency (EMA) on December 16, 2021, gave an EUA to Paxlovid based on interim results. It was demonstrated that Paxlovid reduced hospitalization and death when treated within 5 days of onset of symptom. Only 1% (6/607) of the Paxlovid-treated patients were hospitalized as against 7% (41/612) of those from the placebo-treated arm within 28 days of starting treatment. None of the deaths occurred in the Paxlovid group, but ten deaths were seen in the placebo group. EMA's human medicines committee (CHMP) has also recommended conditional marketing authorization for Paxlovid. The study of CHMP data evaluated patients of COVID-19 who were treated with Paxlovid significantly reduced hospitalization, and it was 0.8% (8/1039) compared to placebo 6.3% (66/1046). Numerous clinical trials of paxlovid are ongoing and are given in [Table 3].
Paxlovid is now available in two dose packs [Table 1]:
- Paxlovid 300 mg; 100 mg dose pack: Contains 3 tablets per dose
- Paxlovid 150 mg; 100 mg dose pack: Contains 2 tablets per dose.
The dosage regimen of the pharmaceutical preparation for the treatment of patients 12 years and older is as follows:
The patient population treatable with paxlovid
Paxlovid is recommended for use in (1) confirmed COVID patients and/or increased risk of severe illness and (2) patients 12 years and older. Its use is not advisable in the following patients: (1) liver/kidney impaired patients; (2) HIV-infected patients; (3) systemic infection other than COVID-19; (4) any patient who has a comorbid condition and requires hospitalization and/or surgery within 7 days before the study or considered life-threatening within 30 days before the study entry; and (5) patients who are pregnant or expected to become pregnant and not using contraception.
Paxlovid: Hopefully an excellent drug for COVID-19 patients
There is a dire need for alternative medicine for corona patients. Paxlovid can be a promising drug because SARS-CoV-2 has single-stranded RNA and a very high transmissibility rate; also it has a higher receptor binding affinity, so more susceptible to protease and can change quickly in alternate host cell receptors. The biochemical nature of the virus shows that it has five types of known variants and its subtypes now alpha, beta, gamma, delta, and omicron (Alpha-B.1.1.7 was first identified in the U.K, Beta B1.351 first identified in South Africa, Gamma P. 1 first identified in Brazil, Delta B.1.617.2 first identified in India, and B.1.1.529-Omicron first distinguished in South Africa and Botswana, are most infected variant among their group)., Coronavirus has the largest genome among all kinds of known RNA viruses. SARS-CoV-2 genome has nonsegmented positive sense-stranded RNA which is about 30 kb in length and contains a 5'cap and 3'poly-A tail structure. This viral genome has 29 encoded proteins; among these, 25 are nonstructural and accessory and 4 are structural proteins. Nonstructural protein plays a very important role in VIRAL RNA replication and invasion in the human immune system and also accessory structure protein is responsible for multiple functions such as viral infection, transmission, and survival in host cell/human cells, whereas structural protein is responsible for assembling and loading the virus particles., Omicron is identified most recent new variant, first reported in South Africa on November 24, 2021, which has 32 mutants. Paxlovid is a broad range spectrum, and the ability to fight against omicron because of its biochemical structure (PF-07321332 and boceprevir) which is a second-generation oral SARS-COV Mpro inhibitor. As the study addressed, Paxlovid is capable of treating infections from multiple coronaviruses which affect the human in vitro such as SARS-COV, SARS-COV-2, HCov-OC43, MERS-COV, HCoV-229E, and HCov-NL63. Owen DR et al, 2021 discovered that PF-07321332 can boost the anti-SARS-CoV-2 activity in animal models (mouse and monkey) without cytotoxic activity and desirable pharmacokinetics and bioavailability properties. Another study suggests that in vitro, Mpro variants (such as G155, T211, L895, K90R, and L205V) are highly susceptible to PF-07321332, and paxlovid is very effective, and the P132H mutant of the omicron variant is not able to perform anti-SARS-CoV 2 activities with Paxlovid. It can destroy the property of Beta and Delta SARS-CoV-2 variants. Hence, we can expect that Paxlovid is a promising effective and safe alternative in the era of the omicron variant. Along with paxlovid, remdesivir, and molnupiravir are also effective, and all these three drugs have different mechanisms of action and proven efficacy in clinical trials in different markers in disease progression.
It is anticipated when Paxlovid is used alone or in combination with molnupiravir (also an antiviral agent) or remdesivir could change the pandemic turbulence worldwide.
Because of this pathogen, the economic burden on the world/hospital/healthcare system is increasing continuously and it will be not sustainable if the progression will continue. Therefore, there is an unmet need for an aggressive approach to control SARS-CoV-2 with early treatment at home at the community level. Paxlovid is cheaper and can be given at home also. Consequently, it reduces the economic burden globally.
| » Discussion and Summary|| |
Paxlovid is an emerging antiviral treatment that is anticipated to be highly beneficial in SARS-CoV-2 infection. It seems very effective in all kinds of corona variants, including new variants such as omicron as it can counter the several S protein mutations in the new variant that are not neutralized by vaccines or other existing drugs. It is comparatively cheaper than other antiviral drugs, available monoclonal antibodies, immunomodulatory agents, or other adjunctive treatments such as remdesivir, tocilizumab, or interleukin-6 inhibitor, respectively. It is to be used cautiously in liver and kidney patients. Moreover, Paxlovid is contraindicated to be used with drugs that are metabolized by CYP3A such as statins, silodosin, antiarrhythmics such as amiodarone and quinine; antipsychotics like clozapine and pimozide; oral midazolam, etc., as it can lead to serious reactions. An example of this is a robust drug–drug interaction between Paxlovid and tacrolimus (metabolized by CYP P450 3A4) when Paxlovid was given to a kidney transplant patient receiving tacrolimus. Furthermore, inducers of CYP3A4 when coadministered with Paxlovid can significantly reduce the plasma concentrations of nirmatrelvir or Paxlovid and may result in reduced antiviral response.
In a recently conducted preclinical study, Paxlovid was shown to accelerate degeneration of cartilage by the activation of endoplasmic reticulum stress and interfering with redox homeostasis. Therefore, a long-term follow-up is recommended to look out for the development of osteoarthritis. Paxlovid has demonstrated favorable outcomes in preclinical studies with minimum genetic toxicity and negative effect. A preclinical study done on male and female rats reported that nirmatrelvir given in very high doses (up to 1000 mg/kg/day, leading to more than 4 times systemic exposure of a human dose) did not affect their fertility, reproductive potential, or early embryonic potential., Moreover, ritonavir too, does not adversely affect fertility as observed in rats, when the exposure was twice that of humans (in males) and 4 times (in females). Moreover, oral antiviral drugs are likely to be safer and quicker in action than existing vaccines or hydroxychloroquine. Another positive aspect is that oral antiviral drugs can be produced on large scale in a shorter period as well with no requirement of refrigeration, shipping, or treatment in the hospital and are less costly than other existing regimens such as monoclonal antibodies, vaccines, or adjuvant drugs.,
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Conflicts of interest
There are no conflicts of interest.
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[Table 1], [Table 2], [Table 3]