Controversy Surrounding Development of E-cigarette-like Devices for Medical Conditions

Aug.12.2024
Controversy Surrounding Development of E-cigarette-like Devices for Medical Conditions
Several US companies developing e-cigarette-like devices for medical conditions face scrutiny from health officials and the public.

According to a recent report by Reuters, several American companies developing devices similar to e-cigarettes to alleviate medical conditions such as migraines and respiratory diseases continue to face skepticism from health authorities and the public. These companies believe that there is still a long way to go before obtaining approval from health departments, and during this period, they will need to demonstrate the effectiveness of their devices.


It has been reported that Qnovia and MIIST Therapeutics have developed nebulizer devices similar to existing medical nebulizers. These devices convert e-liquid medication into aerosol form for inhalation. Additionally, Greentank has claimed to have developed a new device aimed at addressing safety issues with existing nebulizer devices, which can more effectively treat conditions such as migraines. Experts, including Professor Federico Buonocore, a specialist in pulmonary drug delivery at Kingston University in the UK, believe that these advancements in nebulizer technology will greatly benefit patients.


The existing inhalation drug delivery devices are bulky and difficult to operate, often leading to improper use. Designs similar to e-cigarettes can address these challenges.


These companies claim that inhalation can provide faster pain relief with fewer side effects compared to pills. Inhalation therapy can relieve pain within seconds and has fewer side effects than traditional medications. However, the potential harmful effects of inhalation devices are currently hindering the progress of these projects.


According to data from the World Health Organization, approximately three billion people worldwide suffer from migraines. In addition, there are millions of people suffering from asthma or lung diseases that require inhalation medication. The World Health Organization has stated that e-cigarettes may produce harmful chemicals such as formaldehyde and heavy metals, and the long-term effects are still unclear.


Qnovia and MIIST plan to market their products as smoking cessation aids, available through prescription sales. Greentank, on the other hand, will be using their heating element chips for recreational cannabis and nicotine-containing vapor devices. Currently, Greentank is seeking pharmaceutical partners to support the development of their medication management heating element chips.


Qnovia company plans to submit a drug application in the United States soon and is planning to submit an application to the United Kingdom in 2026, with clinical trials expected to begin in September.


According to reports, tobacco companies such as Philip Morris International (PMI) had previously attempted to enter this market but were unsuccessful. Health officials pointed out numerous cases of failed inhalation devices and health issues.


The CEO of Philip Morris International (PMI) stated that the company did not meet its goals last year because it had been overly optimistic about the market acceptance of non-nicotine industries. A inhalable aspirin product developed by the company was also deemed ineffective after clinical trials last year.


We welcome news tips, article submissions, interview requests, or comments on this piece.

Please contact us at info@2firsts.com, or reach out to Alan Zhao, CEO of 2Firsts, on LinkedIn


Notice

1.  This article is intended solely for professional research purposes related to industry, technology, and policy. Any references to brands or products are made purely for objective description and do not constitute any form of endorsement, recommendation, or promotion by 2Firsts.

2.  The use of nicotine-containing products — including, but not limited to, cigarettes, e-cigarettes, nicotine pouchand heated tobacco products — carries significant health risks. Users are responsible for complying with all applicable laws and regulations in their respective jurisdictions.

3.  This article is not intended to serve as the basis for any investment decisions or financial advice. 2Firsts assumes no direct or indirect liability for any inaccuracies or errors in the content.

4.  Access to this article is strictly prohibited for individuals below the legal age in their jurisdiction.

 

Copyright

 

This article is either an original work created by 2Firsts or a reproduction from third-party sources with proper attribution. All copyrights and usage rights belong to 2Firsts or the original content provider. Unauthorized reproduction, distribution, or any other form of unauthorized use by any individual or organization is strictly prohibited. Violators will be held legally accountable.

For copyright-related inquiries, please contact: info@2firsts.com

 

AI Assistance Disclaimer

 

This article may have been enhanced using AI tools to improve translation and editorial efficiency. However, due to technical limitations, inaccuracies may occur. Readers are encouraged to refer to the cited sources for the most accurate information.

We welcome any corrections or feedback. Please contact us at: info@2firsts.com

Major U.S.  Vape Distributor Demand Vape Pays at Least $300,000 for White House Lobbying Amid Enforcement Pressure
Major U.S. Vape Distributor Demand Vape Pays at Least $300,000 for White House Lobbying Amid Enforcement Pressure
New York vape distributor Ecto World, which operates as Demand Vape, hired political consultant Roger Stone to lobby the Executive Office of the President on regulation of vaping and related products while facing state enforcement and multiple lawsuits. Public lobbying disclosures show that Ecto World paid at least $300,000 for the work through June 30, 2026. Separately, New York State announced in March that more than 28,500 pounds of vaping products tied to the company had been seized, while New York City and the state have pursued legal or enforcement actions. Public records do not show that the lobbying directly changed any specific regulatory or enforcement outcome.
Sep.08
Product | JTI Philippines Expands Nordic Spirit Nicotine Pouch Portfolio With Dark Pop and Red Frost
Product | JTI Philippines Expands Nordic Spirit Nicotine Pouch Portfolio With Dark Pop and Red Frost
JTI Philippines has expanded the Nordic Spirit nicotine pouch portfolio in the Philippines with two new variants, Dark Pop and Red Frost. Both products maintain the brand’s tobacco-free nicotine pouch positioning, with Dark Pop featuring a fizzy cola profile with citrus and sweet notes, while Red Frost combines cool mint with sweet red berry flavors. The two variants are now available through Philippine online retail channels.
Aug.18
As JUUL2 Wins FDA Authorization, Harm Reduction Journal Highlights the Role of Real-World Evidence in Nicotine Product Regulation
As JUUL2 Wins FDA Authorization, Harm Reduction Journal Highlights the Role of Real-World Evidence in Nicotine Product Regulation
A commentary published in the international open-access, peer-reviewed Harm Reduction Journal argues that randomized controlled trials remain central to evaluating smoking cessation efficacy but cannot alone capture real-world uptake, complete switching, longer-term use and population impact of non-combustible nicotine products such as e-cigarettes, heated tobacco and nicotine pouches. The authors frame impact as “reach × efficacy” and call for real-world evidence to complement RCTs. Three days after publication, the FDA authorized three JUUL2 products and highlighted complete switching among adult smokers in explaining its decision, providing a timely regulatory backdrop to the debate.
Sep.08
2Firsts Compliance Solutions Hosts PMTA Briefing on FDA Review Signals After JUUL2 Authorization
2Firsts Compliance Solutions Hosts PMTA Briefing on FDA Review Signals After JUUL2 Authorization
Following recent FDA authorizations for JUUL2 and ZYN ULTRA, 2Firsts Compliance Solutions held an online PMTA briefing on Sept. 4 to examine what the decisions may signal about review efficiency, scientific evidence and U.S. market access. Nearly 30 participants from brands, manufacturers, compliance service providers and investment firms joined the discussion.
2Firsts Events
Sep.06
IKE Tech Launches IKE 2.0 Compliance Platform for Nicotine Products
IKE Tech Launches IKE 2.0 Compliance Platform for Nicotine Products
IKE Tech launched IKE 2.0 on September 28, initially targeting nicotine products with a platform that combines user identity verification, product authentication, configurable policy controls and data analytics. Products can be authenticated through direct device integration or NFC smart tags. IKE Tech was formed with participation from Ispire's Aspire North America, Berify and Chemular, with Ispire currently holding a 40% interest. Its age-verification component PMTA was accepted by the FDA in 2025 and remains under review. The company did not disclose customer names, commercial deployment volumes, pricing or revenue tied to IKE 2.0.
News
Sep.29 by 2Firsts Perspectives
Malaysia Police Seize RM12.7 Million in Illegal Vapes and Cigarettes as Probe Points to Sea Shipments From China
Malaysia Police Seize RM12.7 Million in Illegal Vapes and Cigarettes as Probe Points to Sea Shipments From China
Police in Malaysia’s Selangor state seized illegal vape products and contraband cigarettes worth about RM12.7 million (approximately $3 million) in two enforcement operations. According to New Straits Times and The Star, the vape-related operation uncovered 131,036 boxes of vape products, 4,900 bottles of e-liquid and 25,510 vape devices, valued at about RM9.4 million. Police said preliminary investigations indicated that some illegal vape products entered Malaysia through sea shipments from China before moving through storage and distribution networks.
Aug.10