Merck
MERCK & CO., INC Rahway, NJ, USA
(known as MSD outside the United States and Canada)

Effective Nov. 20th, 2023 Caraway Therapeutics, Inc.,
a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)

View the Announcement Visit Merck.com

Blog

Merck to Acquire Caraway Therapeutics, Inc.

Acquisition underscores Merck’s ongoing commitment to developing treatments for neurodegenerative diseases

RAHWAY, N.J., & CAMBRIDGE, Mass.–-Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and Caraway Therapeutics, Inc. announced today that the companies have entered into a definitive agreement under which Merck, through a subsidiary, will acquire Caraway Therapeutics for a total potential consideration of up to $610 million, including an undisclosed upfront payment as well as contingent milestone payments. The upfront payment will be expensed by Merck in the fourth quarter of 2023 and included in non-GAAP results.

“Caraway’s multidisciplinary approach has yielded important progress in evaluating novel mechanisms of modulation of lysosomal function with potential for the treatment of progressive neurodegenerative diseases,” said George Addona, senior vice president, discovery, preclinical development and translational medicine, Merck Research Laboratories. “We look forward to applying our expertise to build upon this work with the goal of developing much needed disease-modifying therapies for these conditions.”

Caraway is a preclinical biopharmaceutical company pursuing innovative approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company has built a pipeline of novel, small-molecule therapeutics for the treatment of genetically defined neurodegenerative and rare diseases.

“This important milestone is a testament to the hard work and dedication of the Caraway team and our mission to develop therapeutics with the potential to alter the progression of devasting neurodegenerative diseases and help patients,” said Martin D. Williams, chief executive officer, Caraway Therapeutics. “This acquisition leverages Merck’s industry-leading research and development capabilities to help further advance our discovery and preclinical programs. We thank and appreciate our investors, including SV Health Investors and its Dementia Discovery Fund, AbbVie Ventures, Amgen Ventures, Eisai Innovation and MRL Ventures Fund for their support.”

Under the terms of the agreement, Merck, through a subsidiary, will acquire all outstanding shares of Caraway with earnout milestones associated with the development of certain pipeline candidates. The Board of Directors of Caraway Therapeutics has approved the transaction. Merck, through its MRL Ventures Fund, has been a shareholder of Caraway Therapeutics since 2018.

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors and its Dementia Discovery Fund, AbbVie Ventures, MRL Ventures Fund, Amgen Ventures, and Eisai Innovation. Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

About Merck

At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.merck.com and connect with us on X (formerly Twitter)FacebookInstagramYouTube and LinkedIn.

Forward-Looking Statement of Merck & Co., Inc., Rahway, N.J., USA

This news release of Merck & Co., Inc., Rahway, N.J., USA (the “company”) includes “forward-looking statements” within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. These statements are based upon the current beliefs and expectations of the company’s management and are subject to significant risks and uncertainties. There can be no guarantees with respect to pipeline candidates that the candidates will receive the necessary regulatory approvals or that they will prove to be commercially successful. If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ materially from those set forth in the forward-looking statements.

Risks and uncertainties include but are not limited to, general industry conditions and competition; general economic factors, including interest rate and currency exchange rate fluctuations; the impact of the global outbreak of novel coronavirus disease (COVID-19); the impact of pharmaceutical industry regulation and health care legislation in the United States and internationally; global trends toward health care cost containment; technological advances, new products and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approval; the company’s ability to accurately predict future market conditions; manufacturing difficulties or delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of the company’s patents and other protections for innovative products; and the exposure to litigation, including patent litigation, and/or regulatory actions.

The company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in the company’s Annual Report on Form 10-K for the year ended December 31, 2022 and the company’s other filings with the Securities and Exchange Commission (SEC) available at the SEC’s Internet site (www.sec.gov).

Contacts

Merck Investor Contact:

Peter Dannenbaum
(908) 447-6900

Merck Media Contacts:

Justine Moore
(347) 281-3754

Olivia Finucane
00 / + 44 7881 262476

Caraway Media Contact:

Carolyn Noyes
CNoyes@macdougall.bio

Caraway Therapeutics to Present at the 33rd Annual Oppenheimer Healthcare Conference

CAMBRIDGE, Mass.–March 08, 2023–Caraway Therapeutics today announced that the Company will be participating in the 33rd Annual Oppenheimer Healthcare Conference on March 13, 2023.

Caraway’s Chief Executive Officer, Martin D. Williams, will present recent advances in the Company’s TRPML1 programs from 4:40pm-5:10pm ET. In addition, the Company will be participating in 1-on-1 investor meetings during the conference.

“Caraway is making great progress on its preclinical TRPML1 programs for the treatment of Parkinson’s and other rare diseases, and I look forward to discussing our work at this event and connecting with investors,” said Williams.

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

Contacts

Media:
MacDougall
Carolyn Noyes
(781) 235-3060
cnoyes@macdougall.bio

Caraway Therapeutics to Present at Two Upcoming Investor Conferences

CAMBRIDGE, Mass. – October 7, 2022 – Caraway Therapeutics today announced that the Company will be participating in two upcoming investor conferences.

Caraway’s Chief Executive Officer, Martin D. Williams, will present recent advances in the Company’s TRPML1 program at the Fall Life Sciences Private Company Showcase, co-hosted by BMO Capital Markets, Solebury Strategic Communications and Goodwin in New York, NY on October 13, 2022, from 4:20pm-4:40pm ET.

Williams will also present at the Oppenheimer Private Company Showcase in Palo Alto, CA on October 18, 2022, from 9:25am-9:45am PT.

“I look forward to sharing the latest updates on Caraway’s work to develop precision medicines for CNS and rare diseases,” said Williams. “We continue to progress our TRPML1 program for GBA-Parkinson’s disease and other rare genetic diseases and are looking forward to discussing our progress with investors.”

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

 

Media Contact:
MacDougall

Kari Watson or Carolyn Noyes
(781) 235-3060

kwatson@macdougall.bio or cnoyes@macdougall.bio

Caraway Therapeutics to Present at The Michael J. Fox Foundation’s Parkinson’s Disease Therapeutics Conference

CAMBRIDGE, Mass. – October 6, 2022 – Caraway Therapeutics today announced that the Company will be presenting new data at The Michael J. Fox Foundation’s Parkinson’s Disease Therapeutics Conference, taking place October 13, 2022, in New York, New York. Magdalene Moran, Ph.D., President & Chief Scientific Officer of Caraway and Donato del Camino, Ph. D., Vice President of Drug Discovery will present the poster “Advancing TRPML1 Agonists for GBA-PD”, detailing the Company’s TRPML1 program currently in preclinical development for GBA-Parkinson’s disease (GBA-PD).

“We are excited to provide updates on our ongoing efforts to develop TRPML1 activators as potential therapeutics for GBA-Parkinson’s disease. Our poster presentation highlights data indicating that TRPML1 activation enhances the activity of the glucocerebrosidase (GCase) pathway and alters the clearance of both disease-relevant lipids and alpha-synuclein, key drivers of GBA-PD disease processes,” said Dr. Moran. “As we continue to advance our TRPML1 GBA-PD program, we are committed to bringing new therapeutic options to patients living with GBA-Parkinson’s disease. We remain grateful to The Michael J. Fox Foundation for their continued support.”

GBA-PD is the most common genetic form of Parkinson’s disease. Patients with GBA mutations tend to have earlier onset of disease, more rapid progression, and a higher risk of dementia than patients with idiopathic PD. Homozygous mutations in glucocerebrosidase, the protein encoded by GBA, cause the lysosomal storage disease, Gaucher disease, indicating that GBA is critical to healthy lysosomal function.

TRPML1 is a non-selective cation channel that contributes to the regulation of lysosomal ionic contents and mediates communication with the rest of the cell. Data suggest that enhancing TRPML1 activity improves lysosomal function, and in previous research Caraway’s TRPML1 activators have enhanced GCase activity and expression in both models of lysosomal storage diseases as well as in autosomal dominant polycystic kidney disease (ADPKD).

Poster presentations will be given throughout the day of the conference. More information on the event can be found at https://www.michaeljfox.org/2022-pd-therapeutics-conference.

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The Company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The Company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments, and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

 

Media Contact:
MacDougall

Kari Watson or Carolyn Noyes
(781) 235-3060

kwatson@macdougall.bio or cnoyes@macdougall.bio

Caraway Therapeutics to Participate in William Blair Biotech Focus Conference

CAMBRIDGE, Mass. — July 06, 2022 — Caraway Therapeutics today announced that the Company will be participating in the William Blair Biotech Focus Conference, taking place July 13, 2022, in New York City. Caraway’s Chief Executive Officer, Martin D. Williams, will participate in a fireside chat with Myles Minter, PhD, Biotech Equity Research Analyst at William Blair, to discuss recent advances in the Company’s lead program targeting the lysosomal cation channel, TRPML1, for the treatment of GBA-Parkinson’s disease (GBA-PD) and other rare genetic diseases.

“We have demonstrated that enhancing TRPML1 function boosts lysosomal function, enhances key lipid recycling pathways that are compromised in GBA-PD patients, and speeds up the clearance of toxic materials that accumulate in a number of genetically defined diseases,” said Williams. “I look forward to speaking with Myles about updates to our TRPML1 program, as well as engaging with investors at the William Blair conference.”

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The Company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The Company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments, and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

Contacts

Media Contact:
MacDougall
Kari Watson or Nicholas Chang
(781) 235-3060
kwatson@macdougall.bio or nchang@macdougall.bio

Caraway Therapeutics to Present at Oppenheimer 32nd Annual Healthcare Conference

CAMBRIDGE, Mass. – March 8, 2022 – Caraway Therapeutics today announced that the Company will be presenting at the Oppenheimer 32nd Annual Healthcare Conference on Tuesday, March 15, 2022 at 9:20am Eastern Time. Caraway’s Chief Executive Officer, Martin D. Williams, will highlight recent advances in the company’s lead program targeting the lysosomal cation channel, TRPML1, for the treatment of GBA-Parkinson’s disease and other rare genetic diseases.

“Caraway is developing oral small molecule therapeutics that enhance lysosomal function to accelerate clearance of toxic materials, such as proteins, oligomers and lipids, that accumulate in many genetically defined neurodegenerative and rare diseases,” said Williams. “I look forward to providing updates on our TRPML1 and pipeline programs at the Oppenheimer conference.”

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

 

Media Contact:
MacDougall

Kari Watson or Nicholas Chang
(781) 235-3060

kwatson@macbiocom.com or nchang@macbiocom.com

 

Caraway Therapeutics Expands Scientific Advisory Board with the Appointment of David Clapham, MD, PhD

– Esteemed Harvard Medical School Professor Emeritus and HHMI Investigator, Dr. David Clapham, brings world class expertise on ciliary ion channel biology –

CAMBRIDGE, MA – March 2, 2022 –  Caraway Therapeutics today announced the appointment of David Clapham, MD, PhD, to the company’s Scientific Advisory Board (SAB). Dr. Clapham is one of the world’s foremost experts in ion channel biology and joins Caraway to advise the Company on its research and development programs.

“I am delighted to welcome Dr. Clapham to Caraway as a scientific advisor,” said Martin D. Williams, Chief Executive Officer at Caraway Therapeutics. “David has decades of expertise interrogating ion channel function and their impact on downstream cell signaling. His lab is a world-leader in the characterization of ciliary ion channels involved in rare genetic diseases, such as nephronophthisis (NPHP), Bardet-Biedl syndrome (BBS), and polycystic kidney disease (PKD). The combined cutting-edge expertise and wisdom David provides will be a key asset for Caraway as we continue to advance our programs.”

David Clapham, MD, PhD is a renowned ion channel biologist whose research focuses on understanding the impact of ion channels on cell signaling pathways and cell physiology. Dr. Clapham is the Aldo R. Castañeda Professor of Cardiovascular Research and professor emeritus of neurobiology at Harvard Medical School. He currently maintains a lab at the Howard Hughes Medical Institute (HHMI) Janelia Research Campus and previously served as HHMI vice president and chief scientific officer. Dr. Clapham was also elected to the National Academy of Sciences in 2006 and the National Academy of Medicine in 2021. He earned his MD and PhD degrees at Emory University School of Medicine. During his residency in Internal Medicine at Brigham and Women’s Hospital, he was a Fulbright fellow with Nobel Prize winner Erwin Neher at the Max Planck Institute for Biophysical Chemistry in Göttingen, Germany.

Dr. Clapham joins Caraway’s experienced, collaborative, and dedicated Scientific Advisory Board team comprised of tenured biologists and biotech leaders.

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

Contacts

MacDougall
Nick Chang or Kari Watson
(781) 235-3060
nchang@macdougall.bio or kwatson@macdougall.bio

 

Caraway Therapeutics Receives Third Research Grant from The Michael J. Fox Foundation to Continue Advancement of TRPML1 Agonists for GBA-Parkinson’s Disease

CAMBRIDGE, MA – January 26, 2022 – Caraway Therapeutics today announced that the Company has been awarded a third research grant from The Michael J. Fox Foundation for Parkinson’s Research (MJFF). This latest grant enables Caraway to further explore the role of TRPML1 activation in alpha-synuclein processing and clearance. It also supports efforts to identify biomarkers for use in clinical trials of the Company’s proprietary TRPML1 agonists in GBA-Parkinson’s disease (GBA-PD). Mutations in the GBA gene disrupt the function of the lysosomal lipid processing enzyme it encodes, glucocerebrosidase (GCase), and are among the most significant genetic risk factors for the development of Parkinson’s disease. Severe homozygous mutations in GBA cause Gaucher disease, a lysosomal storage disorder.

TRPML1, a lysosomal cation channel, regulates the activity of the lysosome, the organelle responsible for recycling cellular debris, such as aggregated alpha-synuclein and toxic lipids. Data suggests that increasing TRPML1 activity improves lysosomal function, addressing the underlying defect in GBA-PD. In previous research, Caraway’s TRPML1 activators have impacted the production of various lipids and alpha-synuclein in neurons derived from patients with GBA-PD. The Company will use the grant funding to further evaluate these effects and characterize potential biomarkers which may be used in future clinical trials of TRPML1 activators.

“It has been a pleasure to work with The Michael J. Fox Foundation and we are thrilled to continue our partnership with this third grant,” said Martin D. Williams, Chief Executive Officer at Caraway Therapeutics. “Understanding the role TRPML1 plays in alpha-synuclein clearance will be important as we advance our TRPML1 program towards the clinic and further our understanding of how our TRPML1 agonists impact disease processes in GBA-PD, one of the most common genetically-defined forms of PD.”

“TRPML1 activation leads to enhanced activity of the GCase pathway which is compromised in GBA-PD patients,” added Magdalene Moran, Chief Scientific Officer at Caraway Therapeutics. “GBA-PD is characterized by lysosomal dysfunction. By agonizing TRPML1, we aim to restore the activity of the lysosome and improve cell health.”

“MJFF continues to invest in research that will improve our understanding of lysosomal function in PD. We are pleased to award this third grant to Caraway to increase our understanding of TRPML1, a target of high interest to the Foundation,” said Marco Baptista, MJFF Vice President of Research Programs.

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique

product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

 

Media Contact:

MacDougall

Nick Chang or Kari Watson (781) 235-3060

nchang@macdougall.bio or kwatson@macdougall.bio

Caraway Therapeutics to Present at Two Upcoming Investor Conferences

CAMBRIDGE, Mass. – November 10, 2021 – Caraway Therapeutics today announced that the Company is scheduled to participate at two upcoming investor conferences.

Caraway’s Chief Executive Officer, Martin D. Williams, will provide a company overview at the Jefferies 12th Annual London Healthcare Conference on November 17, 2021, at 5:00 – 5:35 PM GMT (12:00 – 12:35 PM EST).

Williams will also present at the Piper Sandler 33rd Annual Healthcare Conference taking place November 29 – December 2, 2021. A company presentation will be available to registered attendees via the conference website from November 22 to December 2, 2021.

“We have been focused on building a pipeline of oral small molecule therapeutics aimed at enhancing lysosomal function to activate the cell’s endogenous clearance and recycling processes for the treatment of neurodegenerative and rare diseases,” said Williams. “I look forward to providing updates on our promising programs at the Jefferies and Piper Sandler Healthcare conferences.”

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

 

Media Contact:
MacDougall

Kari Watson or Nicholas Chang
(781) 235-3060

kwatson@macbiocom.com or nchang@macbiocom.com

 

 

Caraway Therapeutics to Present at the Oppenheimer Fall Healthcare Life Sciences & MedTech Summit

CAMBRIDGE, Mass. – September 16, 2021 – Caraway Therapeutics today announced that the Company’s Chief Executive Officer, Martin D. Williams, will present at the virtual Oppenheimer Fall Healthcare Life Sciences & MedTech Summit on Thursday, September 23, 2021 at 2:55pm Eastern Time. The presentation will cover recent progress from Caraway’s lead program targeting modulation of the lysosomal cation channel, TRPML1, for GBA-Parkinson’s disease and other rare diseases, and highlight the recently established collaboration with AbbVie on Caraway’s second program targeting the lysosomal potassium channel, TMEM175, for Parkinson’s and other neurodegenerative diseases.

“I look forward to sharing updates on Caraway’s promising programs at the Oppenheimer healthcare fall summit,” said Williams. “We have made substantial progress on our approach that combines genetically defined targets and our expertise in lysosomal biology to develop oral small molecule therapeutics to address unmet medical needs in neurodegenerative and rare diseases.”

 

About Caraway Therapeutics

Caraway Therapeutics is a biopharmaceutical company pursuing novel approaches for the treatment of genetically defined neurodegenerative and rare diseases. The company is a leader in the cutting-edge science of activating cellular recycling processes to clear toxic materials and defective cellular components by modulating lysosomal function. Caraway is utilizing its unique product engine to develop proprietary insights into lysosomal function and small molecule ion channel modulation and advance a robust pipeline of precision therapeutic candidates with disease-modifying potential for patients. The company is backed by top-tier investors, including SV Health Investors, AbbVie Ventures, MRLV Fund, Amgen Ventures, Dementia Discovery Fund, Alexandria Venture Investments and Eisai Innovation.

Caraway is based in Cambridge, MA. For more information, please visit www.carawaytx.com.

 

Media Contact:
MacDougall

Kari Watson or Nicholas Chang
(781) 235-3060

kwatson@macbiocom.com or nchang@macbiocom.com