Biopharmaceutical company focused on the development and commercialization of treatments for orphan dermatologic diseases.

Joined April 2020
120 Photos and videos
Today we entered into a definitive agreement to be acquired by LEO Pharma @LEOHealthySkin, a wholly-owned subsidiary of LEO Pharma A/S. The transaction is expected to close in the fourth quarter of 2023 subject to closing conditions. See our press release: timberpharma.com/news-releas…
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Today we shared interim pharmacokinetic analyses from the Phase 3 ASCEND study, our pivotal clinical trial for moderate to severe X-linked (RXLI) or lamellar #ichthyosis (ARCI). We plan to present the data at #SPD2023 in July. Find details: timberpharma.com/news-releas…
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Peyton lives with X-linked #ichthyosis, characterized by dry, scaly patches of skin that cover the body. “When I’m not itching, I just feel different. I feel better, because I’m not constantly scratching.” Read more from @FIRST_Skin: firstskinfoundation.org/news…

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We’re grateful for the support of @YaleMed, which has been an integral part of our congenital #ichthyosis development program as the only U.S. site involved in all 3 of our clinical trials. Dr. Chris Bunick talks more about the study in @DermTimes: dermatologytimes.com/view/tm…
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As we recognize the end of #IchthyosisAwarenessMonth, we encourage you to visit @FIRST_Skin to learn more about congenital #ichthyosis and its impact on patients and families: firstskinfoundation.org/
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After developing itchy, painful scales on his skin, Aditya was diagnosed with congenital #ichthyosis (CI) at seven years old. Now, he’s sharing his story to build awareness of this rare genetic skin condition and help others feel less alone. Read more: scarysymptoms.com/2022/09/me…
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Learn more about the ASCEND study, a randomized controlled pivotal Phase 3 clinical trial in patients with autosomal recessive congenital ichthyosis lamellar ichthyosis (ARCI-LI) or X-linked recessive #ichthyosis (XRI). Learn more at ichthyosistrial.com/
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May 20 marks #ClinicalTrialsDay. As we continue to advance our pivotal Phase 3 ASCEND study for congenital #ichthyosis, we thank the site investigators, research staff, patients, caregivers and families who have helped us move this important research effort forward.
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Peyton Fleagle was just a toddler when his parents first noticed itchy scales on his skin. Eventually the scales covered 95% of Peyton's body. @Medical_xpress shares more about our work on behalf of Peyton & all those living with congenital #ichthyosis: medicalxpress.com/news/2023-…
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May is #Ichthyosis Awareness Month, an opportunity to join with patients & families around the world to raise awareness about the challenges & hopes of the ichthyosis community. Learn how you can get involved: firstskinfoundation.org/icht… #IAM23 @FIRST_Skin
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Today we announced the online publication of a sub-analysis of the Phase 2B CONTROL study in Clinical and Experimental Dermatology (CED), the educational journal of the British Association of Dermatologists (@HealthySkin4All). See our press release: timberpharma.com/news-releas…
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We’re grateful to work with patient advocates who are passionate about sharing their stories with their communities to raise awareness of congenital #ichthyosis & opportunities to participate in clinical research. The Fleagle family shares their story: patch.com/connecticut/enfiel…
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The @AADskin Annual Meeting begins today! #AAD2023 will discuss some of the most important topics and latest updates in #dermatology and provide the opportunity to connect with more than 8k members of the clinical and research community. View here: aad.org/member/meetings-educ…
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#ICYMI Last month, we received orphan drug designation for our lead candidate in development for the treatment of X-linked recessive #ichthyosis (XLRI) from the European Commission. Learn more: timberpharma.com/news-releas…
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In an interview with @AuthorityMag, Christina and Peyton share their experiences with X-linked #ichthyosis in an effort to build awareness of this rare genetic skin disorder: medium.com/authority-magazin…
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Aditya was recently interviewed as part of @AuthorityMag’s #Unstoppable series, where he shared his story & talked about his work as a patient advocate and desire to help others living with congenital #ichthyosis. Read now: medium.com/authority-magazin…
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Today we recognize #RareDiseaseDay and show our support for the 300 million individuals impacted by #rarediseases worldwide, including #ichthyosis. Join us today in celebrating #RDD2023 with @First_Skin: firstskinfoundation.org/news…
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