Revance Therapeutics

Revance Therapeutics Revance is a biotechnology company setting the new standard in healthcare with innovative aesthetic

We value speed, audacity, authenticity, grit, and empathy, and empower our teams to reimagine the status quo.

01/06/2023

Today, announced that the FDA has accepted the supplemental Biologics License Application for DAXXIFY® (daxibotulinumtoxinA-lanm) for injection for the treatment of cervical dystonia in adults. Cervical dystonia is a chronic and debilitating neurologic condition affecting the muscles of the neck and based on the results from Revance’s Phase 3 cervical dystonia clinical development program, is generally safe, efficacious, and demonstrates a long duration of efficacy, potentially reducing the risk of symptom re-emergence between treatments. This milestone advances Revance’s potential in therapeutics and reinforces the possible benefits of DAXXIFY® in muscle movement disorders. To learn more, visit https://investors.revance.com/news-releases/news-release-details/revance-announces-us-fda-acceptance-supplemental-biologics

11/24/2022

On this day, we express our gratitude to all employees, practice partners and stakeholders. From the Revance family to yours, Happy Thanksgiving!

Thank you to our servicemen and women. This  , Revance thanks you for your commitment, bravery, and sacrifices to keep u...
11/11/2022

Thank you to our servicemen and women. This , Revance thanks you for your commitment, bravery, and sacrifices to keep us safe at home and abroad.

Introducing our Fall intern class of 2022! Thank you for all your hard work and dedication in   here at Revance.        ...
10/14/2022

Introducing our Fall intern class of 2022! Thank you for all your hard work and dedication in here at Revance.

10/10/2022

Valuable insight was shared at the 2022 American Society for Dermatologic Surgery meeting in Denver, CO! To learn more about Revance's latest findings on DAXXIFY™, please visit - https://bit.ly/3STSmqc

10/06/2022

is proud to announce the publication of two peer-reviewed articles on DAXXIFY™ (daxibotulinumtoxinA-lanm) injection for the treatment of glabellar lines in the Aesthetic Surgery Journal.



Watch for Important Safety Information. For Full Prescribing Information including Boxed Warning and Medication Guide, see https://bit.ly/3QqQxPm

DAXXIFY™ is a prescription medicine for adults to temporarily improve the look of moderate to severe frown lines between the eyebrows. Ask your doctor to tell you about DAXXIFY™. DAXXIFY™ may cause serious side effects hours to weeks after injection. Alert your doctor right away as difficulty swallowing, speaking, breathing, eye problems or muscle weakness can be a sign of a life-threatening condition. The most common side effects are headache, eyelid drooping, and loss of the ability to move some muscles in your face.

Call your doctor for medical advice about side effects. Intended for US audiences.

This just in!   has been buzzing in the news lately. Visit https://www.revance.com/news to read the latest headlines on ...
09/29/2022

This just in! has been buzzing in the news lately. Visit https://www.revance.com/news to read the latest headlines on our award-winning .

  is pleased to announce that  , the first relational commerce platform for aesthetic practices, has been selected by Oc...
09/27/2022

is pleased to announce that , the first relational commerce platform for aesthetic practices, has been selected by Octane OC as a finalist in the annual 2022 Awards for the best innovation in the enterprise / B2B technology category

Last week,   celebrated the FDA approval of DAXXIFY™ (daxibotulinumtoxinA-lanm) injection, positioning the company to di...
09/12/2022

Last week, celebrated the FDA approval of DAXXIFY™ (daxibotulinumtoxinA-lanm) injection, positioning the company to disrupt the $3.2B U.S. facial injectables market. To mark the occasion, was featured on the NASDAQ tower in Times Square in NYC!

For Full Prescribing Information including Boxed Warning and Medication Guide, see https://bit.ly/3QqQxPm DAXXIFY is a prescription medicine for adults to temporarily improve the look of moderate to severe frown lines between the eyebrows. Ask your doctor to tell you about DAXXIFY. DAXXIFY may cause serious side effects hours to weeks after injection. Alert your doctor right away as difficulty swallowing, speaking, breathing, eye problems or muscle weakness can be a sign of a life-threatening condition. The most common side effects are headache, eyelid drooping, and loss of the ability to move some muscles in your face. Call your doctor for medical advice about side effects. Intended for US audiences.

09/08/2022

Finally, the long-lasting, peptide-powered frown line treatment your patients have been wanting is now approved! DAXXIFY™ (daxibotulinumtoxinA-lanm) injection is the first and only peptide-powered, FDA-approved frown line treatment with a median duration of 6 months and up to 9 months for some patients.*

Experience the future of aesthetics with –coming soon for exclusive providers. Visit https://bit.ly/3D4w8Ni to learn more about partnering with us.

Tap the share icon to spread the news about DAXXIFY™–the only long-lasting, peptide-powered frown line treatment.



Watch for Important Safety Information. For Full Prescribing Information, including Boxed Warning and Medication Guide, see https://bit.ly/3QqQxPm

DAXXIFY™ is a prescription medicine for adults to temporarily improve the look of moderate to severe frown lines between the eyebrows. Ask your doctor to tell you about DAXXIFY™. DAXXIFY™ may cause serious side effects hours to weeks after injection. Alert your doctor right away as difficulty swallowing, speaking, breathing, eye problems or muscle weakness can be a sign of a life-threatening condition. The most common side effects are headache, eyelid drooping, and loss of the ability to move some muscles in your face.

Call your doctor for medical advice about side effects. Intended for US audiences.

*At least 50% of patients in SAKURA 1 and SAKURA 2 had none or mild frown lines for 24 weeks (6 months) and 23.9 weeks (6 months) or longer, respectively, per both investigator's and patient's assessments. 5% of patients in SAKURA 1 and 3% of patients in SAKURA 2 had none or mild frown lines at 9 months per investigator’s assessment. In SAKURA 1, SAKURA 2, and SAKURA 3 OLS Treatments 1 and 2, 7.5%, 5.4%, 17.4%, and 11.6% of patients, respectively, had not returned to baseline severity at 9 months per both investigator’s and patient’s assessments.

Thank you to all of our staff, partners, and customers for the incredible work you do. We wish you a relaxing Labor Day!
09/05/2022

Thank you to all of our staff, partners, and customers for the incredible work you do. We wish you a relaxing Labor Day!

Address

1222 Demonbreun Street, 20th Floor
Nashville, TN
37203

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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