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The femtech pioneers revolutionising contraception

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Since the pill was invented in the 1960s, there has been little progress in the world of female contraception, and many of the methods currently on the market come with unwanted side effects. With the rise of femtech, however, comes renewed focus on providing contraceptive solutions that work for women. 

When it comes to contraception, the options for women haven’t changed for decades. From the hormonal pill to the IUD implant, many come with unwanted side effects and are not suitable for everyone.

Furthermore, women’s healthcare, of which contraception is a key part, has historically been under-funded and under-researched.

It’s a market ripe for disruption and innovation, which is exactly what the new breed of femtech pioneers are doing.

Period tracking apps

Tech to track menstrual cycles and symptoms is popular with both those women who are planning to conceive and those who definitely aren’t.

While tracking cycle lengths and ovulation times can help women decode the best time to get pregnant, it can also help those women who want a less invasive method of contraception, without having to use hormones.

One such app is Clue, one of the earliest entrants into the period tracking space, with around 13 million people. The team behind the app are preparing to launch a digital contraceptive, which will use a statistical prediction of ovulation as a birth control tool. This will let users know when they are more likely to fall pregnant so they can use birth control or abstain.

In the same vein is Natural Cycles, billed as the world’s first and only CE and FDA approved hormone-free, digital contraception solution.

With 1.5 million registered users it has shown to be 93 per cent effective with typical use, which rose to 98 per cent with perfect use – a similar level to the Pill, with none of the side effects.

Home delivery

In the US, access to contraception can be difficult, especially in more rural areas; around 1.5 million American women live in a county without a single health centre offering the full range of methods.

And the problem was only exacerbated during the Covid-19 lockdowns.

During the pandemic, digital health practice Nurx experienced a surge in requests for at-home delivery of contraception, with a 50 per cent spike in birth control requests, and 40 per cent for emergency contraception.

Following an initial online consultation, the firm delivers most types of birth control, from pills, rings, shots, and patches. It also offers an overnight home delivery of the morning-after pill, an emergency contraceptive that can help reduce chances of pregnancy if taken within three days of unprotected sex.

The perfect match

There are nearly 250 types of contraception available, so it can be hard for women (and prescribers) to have the time to find the right one.

London-based femtech start-up Tuune’s research found that 85 per cent of women did not feel that their doctor spent enough time to find the best birth control for them, 52 per cent of women, globally, experience side effects from their birth control, and 43 per cent of women believe they have a hormone imbalance but can’t get a doctor to diagnose it.

These findings were the catalyst for its innovative product, which uses AI and biological testing to match women with the most suitable contraception for them.

A topical treatment

Away from apps and deliveries, merging technologies have also found a new way to prevent pregnancy, in what its founders say is the biggest revolution in contraception since the Pill.

Copenhagen-based start-up Cirqle Biomedical has developed mucus engineering as a new alternative to hormonal birth control.

The first product based on the technology, named OUI, aims to be as effective as the pill with minimal side effects. It works by using small biopolymers to reinforce the natural mucus barrier in the cervix to make it impenetrable to sperm, preventing it from passing through the cervix and fertilising an egg.

The biopolymer used is derived from either mushrooms or the shell of crustaceans and is known to be biodegradable, non-toxic and already used in other FDA-approved medical devices.

An animal study demonstrated 100 per cent effectiveness and the firm is looking to start human trials in the near future.

Review platform

Contraceptive side effects are common, yet often not talked about or highlighted by medics. The Lowdown, an online review platform for contraception, aims to change that and allow women to make an informed choice.

It was developed by Alice Pelton, who, after being prescribed the Pill at 16, suffered a decade of mood swings before she connected her emotional state with her medication.

By collecting huge amounts of data through user-generated feedback, the site also allows women to check any symptoms they may be experiencing against their method of contraception, and search for alternatives by connecting users with expert advice.

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Congress urged to invest over $20bn to close women’s health gap

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Congress is being urged to invest US$20bn over 10 years to close the women’s health gap.

The American College of Obstetricians and Gynecologists, the Society for Women’s Health Research and the Women First Research Coalition have unveiled the National Strategy to Close the Women’s Health Gap.

The framework calls for a coordinated national effort to improve women’s health research, care and outcomes.

It says women make up more than half of the US population, but their health needs across conditions and life stages have been understudied and underserved for decades.

Kathryn Schubert, president and chief executive of the Society for Women’s Health Research, said: “The women’s health gap has persisted for far too long.

“This strategy offers Congress a road map to improve health outcomes, drive innovation, and build a healthier future for women, families, and communities.”

The strategy notes that Congress required women to be included in National Institutes of Health-funded clinical research through the NIH Revitalization Act in 1993.

However, it says major gaps remain in women’s health research, clinical care and how evidence is put into practice.

The plan proposes US$7bn for research and innovation, including expanded federal investment in women’s health research across the NIH, VA, DoD and the Advanced Research Projects Agency for Health.

It would also establish a Women’s Health Research Interdisciplinary Fund at the NIH and create a national network of Women’s Health Centers of Excellence.

The centres would aim to accelerate the translation of research into clinical care and serve as training sites for researchers and clinicians.

A further US$1bn would be used for regulatory coordination and modernisation, including cross-agency collaboration and work to address sex differences in drug and treatment approvals.

Sex differences are biological differences between females and males that can affect disease risk, symptoms, treatment response and side-effects.

The funding would also support updated NIH tracking systems for women’s health research investment and publication standards on how sex as a biological variable is considered in research.

The strategy calls for US$4bn for data and evidence infrastructure, including a public-private partnership focused on women’s midlife health data.

It would also convene a public workshop to review existing women’s health research datasets and develop common data elements to fill gaps and make datasets more widely available.

Another US$7bn would go towards strengthening the clinical and research workforce.

This would include career pathways, loan repayment programmes, a women’s health clinical workforce loan repayment programme modelled on the National Health Service Corps and interdisciplinary training.

The workforce measures would include particular emphasis on rural and underserved areas.

The final US$1bn would support public awareness and education campaigns to improve health literacy, preventive care and participation in women’s health research.

Health literacy means a person’s ability to find, understand and use health information to make decisions about care.

The campaigns would use digital and traditional media developed in consultation with patient advocacy organisations and relevant medical societies.

Sandra E Brooks, chief executive of the American College of Obstetricians and Gynecologists, said: “Closing the women’s health gap requires not only funding research, but also investment in the people who conduct that research and those who translate research findings and discoveries into better patient care.

“Strengthening the women’s health research and clinical workforce is critical to accelerating the innovation needed to improve health outcomes for women.”

The strategy says women have higher annual out-of-pocket healthcare costs than men and live 25 per cent of their lives in poorer health.

Supporters say this strengthens the economic and public health case for long-term congressional investment.

The framework has been endorsed by organisations across women’s health, ageing, heart disease, autoimmune disease, cancer, reproductive medicine and neurological conditions, including the Women’s Alzheimer’s Movement at Cleveland Clinic, the National MS Society and UsAgainstAlzheimer’s.

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Stardust period tracker shares health data, study reveals

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Stardust shared sensitive period tracking data with third-party analytics firms, according to new privacy research from Mozilla.

The findings expose a privacy divide in femtech, where users often trust apps with highly sensitive reproductive health information.

The research was carried out by Mozilla’s Privacy Not Included team, which tested several period tracking apps.

It found that Stardust, a period tracker used by millions, shared users’ reproductive health data with analytics companies, a practice the research said contrasted with its privacy-first marketing.

Analytics companies collect and examine information about how people use digital products, often to help businesses understand user behaviour or improve marketing.

The findings raise questions about whether privacy promises made by health apps match what happens to users’ data.

According to research reported by TechCrunch, one other period tracking app tested by Mozilla received what researchers called a “squeaky clean” rating, suggesting similar services can operate without sharing sensitive health data in the same way.

Period tracking apps have come under greater scrutiny in the US since the 2022 overturning of Roe v Wade, which removed federal constitutional protection for abortion.

Some users and privacy advocates have warned that menstrual and reproductive health data could potentially be sought in legal cases.

The research also points to a broader regulatory problem for consumer health apps.

In the US, many health apps are not covered by HIPAA, the health privacy law that applies to medical providers and some healthcare organisations.

That means some consumer apps may be able to collect, share or monetise sensitive health data under rules that differ from traditional healthcare privacy protections.

The femtech market, estimated in the report at US$50bn, has grown quickly, but privacy regulation has not always kept pace with app development.

Stardust had not publicly responded to Mozilla’s findings at the time of the original report, and its privacy policy remained live on its website.

The issue is particularly sensitive for period tracking because the data can reveal patterns around fertility, pregnancy, contraception and reproductive health.

Mozilla’s wider Privacy Not Included initiative has examined consumer technology products for privacy and security concerns since launching in 2017, including connected devices, children’s toys and health apps.

The findings come as US lawmakers continue to debate stronger federal privacy rules for sensitive health information collected by consumer apps.

The American Data Privacy and Protection Act, which has been stalled in Congress since 2023, includes provisions addressing sensitive health information collected by consumer apps.

Experts have also warned that anonymised health data can sometimes be re-identified when combined with other information, such as location data.

Re-identification means linking supposedly anonymous data back to a specific person.

A 2019 study found that menstrual cycle data combined with location information could identify individual users with high accuracy.

State-level privacy laws in places such as California, Virginia and Colorado have also given consumers new rights around personal data, although enforcement can vary.

Privacy advocates say the research underlines the need for clearer data practices, stronger safeguards and greater transparency in femtech.

For users, the findings are a reminder that health apps do not automatically protect health information in the same way as healthcare providers.

The report suggests period tracker companies that put privacy first may be better placed to build trust in a market where long-term use depends on confidence.

Mozilla’s investigation suggests privacy promises in femtech do not always match practice, and that period trackers can function without sharing sensitive user data in the same way.

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Juno Bio secures US$3.8m for precision diagnostics

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Juno Bio has secured US$3.8m to expand its diagnostics platform for vaginal health and reproductive care.

The funding round was led by Ada Ventures, with participation from Artesian, Entrepreneur First and Illumina Accelerator.

The women’s health startup said the seed funding will support the launch of its first CLIA-certified sequencing laboratory in Oakland, California, and a new clinical vaginal microbiome and STI test for healthcare providers.

CLIA certification refers to US laboratory standards for testing human samples used in diagnosis, prevention or treatment decisions.

Dr Leighton Turner, co-founder and chief scientific officer of Juno Bio, said: “The vaginal microbiome is still one of the least understood systems in the body at a clinical scale.

“With our lab, we’re starting to build a measurement standard that clinicians can actually use.

“We believe the level of detail from this kind of testing can meaningfully improve how vaginal healthcare is provided.”

The company is developing precision diagnostics for vaginal health, where patients can experience recurring symptoms, inconsistent diagnoses and treatments based on trial and error.

Juno Bio said bringing testing in-house gives it greater control over the process, from sample handling to results, while allowing it to refine its technology and build what it says is one of the largest datasets focused on the vaginal microbiome.

The vaginal microbiome is the community of bacteria and fungi that naturally live in the vagina. Changes in this balance can be linked to infections, symptoms and wider reproductive health issues.

Juno Bio’s newly launched clinical test examines the wider vaginal microbiome and screens for four common sexually transmitted infections, or STIs.

Rather than looking for a single cause, the test is intended to give clinicians a broader picture of what may be contributing to symptoms.

Juno Bio says this matters because multiple infections can occur at the same time and microbiome changes may be linked to fertility, menopause or recurrent infections.

Dr Anna Powell of Johns Hopkins said: “Vaginal microbiome testing has the potential to significantly reshape how we understand and manage vaginal health, particularly for patients with recurrent or unexplained symptoms.

“While the field is still evolving, advances in sequencing and data interpretation are moving us closer to a future where more personalised, microbiome-informed care can complement existing diagnostic approaches.”

Check Warner, co-founding partner at Ada Ventures, added: “Juno Bio is setting a new standard for how vaginal health is understood and managed.

“What they’ve built at this stage, with this level of capital efficiency, is exceptional.

“We’re proud to support the team as they scale their clinical infrastructure and continue leading innovation in this critically underserved category.”

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