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Scholar Rock Announces New Preclinical Data for SRK-439 Showing Significant Lean Mass Increase and Enhanced Fat Mass Loss with Metformin

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Scholar Rock (NASDAQ: SRRK) announced new preclinical data for SRK-439, showing significant lean mass increase and enhanced fat mass loss when combined with metformin. In young mice, the combination treatment demonstrated a 31.6% increase in lean mass compared to 15.1% in controls, while older mice showed a 10.2% increase versus 0.2% in controls. The study also revealed lower fat mass gain in young mice receiving the combination treatment (68.2% increase) compared to metformin alone (114% increase). These results support the potential of selective myostatin inhibition in improving body composition for obesity treatment. The company's Phase 2 EMBRAZE trial is on track for readout in Q2 2025.

Scholar Rock (NASDAQ: SRRK) ha annunciato nuovi dati preclinici per SRK-439, che mostrano un significativo incremento della massa magra e una maggiore perdita di massa grassa quando combinato con la metformina. Nei topi giovani, il trattamento combinato ha dimostrato un 31,6% di aumento della massa magra rispetto al 15,1% nei controlli, mentre i topi più anziani hanno mostrato un 10,2% di aumento rispetto allo 0,2% nei controlli. Lo studio ha inoltre rivelato un minore aumento di massa grassa nei topi giovani che ricevevano il trattamento combinato (68,2% di aumento) rispetto a quelli trattati solo con metformina (114% di aumento). Questi risultati supportano il potenziale dell'inibizione selettiva della miosina nel migliorare la composizione corporea per il trattamento dell'obesità. La fase 2 dello studio EMBRAZE dell'azienda è in programma per la lettura nel secondo trimestre del 2025.

Scholar Rock (NASDAQ: SRRK) anunció nuevos datos preclínicos para SRK-439, que muestran un aumento significativo de la masa magra y una mayor pérdida de masa grasa cuando se combina con metformina. En ratones jóvenes, el tratamiento combinado demostró un 31,6% de aumento en la masa magra en comparación con el 15,1% en los controles, mientras que los ratones mayores mostraron un 10,2% de aumento frente al 0,2% en los controles. El estudio también reveló un menor aumento de masa grasa en los ratones jóvenes que recibieron el tratamiento combinado (68,2% de aumento) en comparación con aquellos que solo recibieron metformina (114% de aumento). Estos resultados respaldan el potencial de la inhibición selectiva de la miosina en la mejora de la composición corporal para el tratamiento de la obesidad. El ensayo EMBRAZE de fase 2 de la compañía está en camino de ser leído en el segundo trimestre de 2025.

스칼라 록 (NASDAQ: SRRK)SRK-439에 대한 새로운 전임상 데이터를 발표하며, 메트포르민과 결합했을 때 상당한 제지방 증가와 지방량 감소가 나타났습니다. 젊은 생쥐에서 이 조합 치료는 제어군의 15.1%에 비해 31.6%의 제지방 증가를 보였고, 노인 생쥐는 제어군의 0.2%에 비해 10.2%의 증가를 보였습니다. 이 연구는 또한 결합 치료를 받은 젊은 생쥐에서 지방량 증가가 메트포르민 단독 치료(114% 증가)와 비교하여 더 낮은 수치(68.2% 증가)임을 밝혔습니다. 이러한 결과는 비만 치료를 위한 신체 구성 개선에 있어 선택적 마이오스타틴 억제의 잠재력을 지지합니다. 회사의 2상 EMBRAZE 시험은 2025년 2분기에 결과 발표를 위해 준비 중입니다.

Scholar Rock (NASDAQ: SRRK) a annoncé de nouvelles données précliniques pour SRK-439, montrant une augmentation significative de la masse maigre et une perte accrue de masse grasse lorsqu'il est combiné avec de la metformine. Chez des souris jeunes, le traitement combiné a révélé une augmentation de 31,6% de la masse maigre, contre 15,1% dans les groupes témoins, tandis que les souris plus âgées ont montré une augmentation de 10,2% contre 0,2% dans les contrôles. L'étude a également révélé un gain de masse grasse inférieur chez les jeunes souris recevant le traitement combiné (augmentation de 68,2%) par rapport à celles recevant uniquement la metformine (augmentation de 114%). Ces résultats soutiennent le potentiel de l'inhibition sélective de la myostatine dans l'amélioration de la composition corporelle pour le traitement de l'obésité. L'essai de phase 2 EMBRAZE de l'entreprise est programmé pour un rendu au deuxième trimestre 2025.

Scholar Rock (NASDAQ: SRRK) hat neue präklinische Daten für SRK-439 veröffentlicht, die einen signifikanten Anstieg der fettfreien Masse und einen verbesserten Fettverlust bei Kombination mit Metformin zeigen. Bei jungen Mäusen zeigte die Kombinationsbehandlung einen 31,6% Anstieg der fettfreien Masse im Vergleich zu 15,1% in der Kontrollgruppe, während ältere Mäuse einen 10,2% Anstieg gegenüber 0,2% in der Kontrollgruppe zeigten. Die Studie ergab auch einen geringeren Anstieg der Fettmasse bei jungen Mäusen, die die Kombinationstherapie erhielten (68,2% Anstieg) im Vergleich zu Metformin allein (114% Anstieg). Diese Ergebnisse unterstützen das Potenzial einer selektiven Myostatin-Hemmung zur Verbesserung der Körperzusammensetzung für die Behandlung von Adipositas. Die Phase-2-Studie EMBRAZE des Unternehmens steht im zweiten Quartal 2025 zur Auswertung an.

Positive
  • Significant lean mass increase demonstrated in preclinical studies (31.6% in young mice, 10.2% in older mice)
  • Reduced fat mass gain observed in combination with metformin (68.2% vs 114% in young mice)
  • Phase 2 EMBRAZE trial progressing as planned with readout expected Q2 2025
Negative
  • Results in older mice showed non-statistically significant fat mass reduction
  • Data to preclinical stage, requiring further validation in humans

Insights

The preclinical data for SRK-439 demonstrates compelling efficacy in improving body composition, particularly when combined with metformin. The key findings show a 31.6% increase in lean mass in young animals and a remarkable 10.2% increase in older animals when treated with SRK-439 and metformin, compared to minimal gains in control groups. The data is particularly significant as it shows effectiveness across different age groups.

The combination therapy also showed promising results in fat mass management, with young mice showing significantly lower fat mass gain (68.2% vs 114%) compared to metformin alone. This dual benefit of increasing lean mass while controlling fat mass gain positions SRK-439 as a potentially valuable therapeutic option for obesity and metabolic disorders.

The upcoming Phase 2 EMBRAZE trial results in Q2 2025 will be important in validating these preclinical findings in humans. The selective myostatin inhibition approach appears to have advantages over broader pathway inhibition, potentially offering better efficacy and safety profiles.

This preclinical data strengthens Scholar Rock's position in the rapidly growing obesity treatment market. With obesity affecting millions globally and the current market lacking treatments that simultaneously address muscle mass and fat reduction, SRK-439 could capture significant market share if human trials replicate these results.

The combination approach with metformin is strategically important, as metformin is widely prescribed for type 2 diabetes and pre-diabetes. This creates a large potential patient population that could benefit from the combination therapy. The positive data across different age groups also expands the potential market reach.

While the Phase 2 EMBRAZE trial results are still over a year away, these preclinical results provide a strong foundation for Scholar Rock's obesity program and could attract partnership interest from larger pharmaceutical companies looking to expand their metabolic disease portfolios.

- Preclinical data show that SRK-439 increased lean mass and lowered fat mass gain in mice receiving metformin

- Data support that Scholar Rock’s unique approach to selective myostatin inhibition could improve body composition in people living with obesity and on an existing background treatment

- Scholar Rock’s industry-leading anti-myostatin portfolio includes SRK-439 and apitegromab, the first investigational anti-myostatin therapy to show improved motor function in Spinal Muscular Atrophy (SMA) in a Phase 3 trial

- Obesity program progressing with Phase 2 EMBRAZE trial on track for readout in Q2 2025

CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Scholar Rock (NASDAQ: SRRK), a late-stage biopharmaceutical company focused on advancing innovative treatments for spinal muscular atrophy (SMA), cardiometabolic disorders, and other serious diseases where protein growth factors play a fundamental role, today announced new preclinical data that support the potential of SRK-439, a highly selective investigational antimyostatin antibody, to increase lean mass and lower fat mass gain when taken with metformin. These data will be presented by Melissa Fulham, Ph.D., of Scholar Rock, at the ObesityWeek conference in San Antonio, Texas on November 5.

“These new data build upon a robust body of evidence demonstrating the potential of selective myostatin inhibition as an important therapeutic approach,” said Jay Backstrom, M.D., MPH, President and Chief Executive Officer at Scholar Rock. “These latest SRK-439 data support our hypothesis that a highly selective approach to targeting myostatin inhibition could have positive effects on body composition in people living with obesity and associated comorbidities like diabetes, and also underscore the value within Scholar Rock’s platform. We are looking forward to providing more updates on the exciting advancements in our cardiometabolic program, including our Phase 2 EMBRAZE trial topline data in the second quarter of 2025.”

Preclinical study design

The research study tested a murine equivalent of SRK-439 in a diet-induced obesity (DIO) mouse model. All mice were given a high-fat diet, followed by either metformin (50 mg/kg daily) or control (water) for four weeks. Following that four-week period, mice in metformin and control groups were given either an IgG control antibody (10 mg/kg weekly) or SRK-439 (10 mg/kg weekly for younger mice and 3 mg/kg weekly for older mice) for another four weeks. To assess whether effects were persistent across age ranges, this study design was repeated in two age groups: both young (10-week-old) and mature (22-week-old) DIO mice.

Quantitative nuclear magnetic resonance (qNMR) was used to analyze change in lean mass at baseline, after four weeks of metformin treatment, and every two weeks following treatment with SRK-439 or IgG control.

Changes in body composition in the presence or absence of metformin

The group that received SRK-439 on the background of metformin showed a significant increase in lean mass versus the group receiving metformin alone, and this result was consistent across age groups. Key findings supporting the potential for SRK-439 in advancing healthier weight management include:

  • Young animals treated with SRK-439 and metformin demonstrated a 2-fold increase in lean mass over the duration of the study compared to the lean mass increase in the metformin group and in IgG controls (31.6% increase from baseline vs. 15.1%, p<0.0001).
  • In older metformin-treated animals, the increase in lean mass in the SRK-439 treated animals compared to IgG controls was 50-fold (10.2% lean mass increase from baseline versus 0.2% in IgG controls, p<0.0001), owing primarily to the limited lean mass growth in the IgG control group over the duration of the study due to the age of the animals.
  • In young mice, the combination treatment of SRK-439 and metformin also resulted in lower fat mass gain (68.2% increase from baseline) than metformin alone (114% increase from baseline; p<0.05).
  • In older mice, SRK-439 showed a trend toward reduced fat mass gain when combined with metformin, as compared to metformin alone (10.6% increase from baseline vs 18.4%; not statistically significant).

“These new preclinical data show that selectively inhibiting myostatin in combination with metformin increased lean mass—and this effect was robust even in the older treatment group that was more weight stable,” said Mo Qatanani, PhD, Chief Scientific Officer at Scholar Rock. "In addition, we observed that when we combined SRK-439 and metformin in younger mice, the effect of lowering fat mass gain was greater than with either therapy alone. Taken together, this is compelling evidence suggesting that SRK-439 has the potential to improve body composition and contribute to healthier weight management in the context of both obesity and type 2 diabetes. These exciting data advance the science of obesity research and continue to differentiate Scholar Rock’s pipeline and anti-myostatin programs.”

Poster Presentation Information
Title: SRK-439 Selectively Inhibits Myostatin to Promote Healthy Body Composition During Metformin Therapy
Presentation type: Poster presentation
Presenter: Melissa Fulham, Ph.D., Senior Scientist II, Scholar Rock
Date and time: Tuesday, November 5, 2024, 2:30 PM CT
Location: Henry B. González Convention Center, San Antonio, TX

For conference information, visit https://obesityweek.org/.

The slides from the presentation are available in the Publications & Posters section of Scholar Rock’s website.

About EMBRAZE

EMBRAZE is a randomized, double-blind, placebo-controlled, Phase 2 proof-of-concept trial evaluating the efficacy, safety and pharmacokinetics of apitegromab in adults with a body mass index (BMI) of >27 (overweight) or a BMI of >30 (obese) and taking a GLP-1 RA (tirzepatide or semaglutide). The target enrollment of EMBRAZE is 100 subjects aged 18-65 who are overweight or obese without diabetes. As part of the study design, the treatment period is 24 weeks, and all subjects will receive a GLP-1 RA. In addition, all subjects will be randomized 1:1 to receive either apitegromab or placebo by intravenous (IV) infusion every four weeks during the 24-week treatment period. The primary endpoint is change from baseline at Week 24 in lean mass assessed by dual-energy X-ray absorptiometry. Secondary endpoints include additional weight loss measures, safety and tolerability, and pharmacokinetic outcomes. Exploratory endpoints at Weeks 24 and 32 include cardiometabolic parameters (e.g. HbA1c), body composition, and physical function.

About SRK-439

SRK-439 is a novel, preclinical, investigational myostatin inhibitor that binds to pro- and latent myostatin with high affinity and is selective for myostatin (i.e., no GDF11 or Activin-A binding), and is initially being developed for the treatment of cardiometabolic disorders, including obesity. Based on preclinical data, SRK-439 has the potential to support healthier weight management by preserving lean mass during weight loss. The efficacy and safety of SRK-439 have not been established and SRK-439 has not been approved for any use by the FDA or any other regulatory agency.

About Apitegromab
Apitegromab is an investigational fully human monoclonal antibody inhibiting myostatin activation by selectively binding the pro- and latent forms of myostatin in the skeletal muscle. It is the first muscle-targeted treatment candidate to demonstrate clinical proof-of-concept in spinal muscular atrophy (SMA). Myostatin, a member of the TGFβ superfamily of growth factors, is expressed primarily by skeletal muscle cells, and the absence of its gene is associated with an increase in muscle mass and strength in multiple animal species, including humans. Scholar Rock believes that its highly selective targeting of pro- and latent forms of myostatin with apitegromab may lead to a clinically meaningful improvement in motor function in patients with SMA. The U.S. Food and Drug Administration (FDA) has granted Fast Track, Orphan Drug and Rare Pediatric Disease designations, and the European Medicines Agency (EMA) has granted Priority Medicines (PRIME) and Orphan Medicinal Product designations, to apitegromab for the treatment of SMA. Apitegromab has not been approved for any use by the FDA or any other regulatory agency.

About Scholar Rock
Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, Scholar Rock has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role.

This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about our approach at ScholarRock.com and follow @ScholarRock and on LinkedIn.

Availability of Other Information About Scholar Rock
Investors and others should note that we communicate with our investors and the public using our company website www.scholarrock.com, including, but not limited to, company disclosures, investor presentations and FAQs, Securities and Exchange Commission filings, press releases, public conference call transcripts and webcast transcripts, as well as on Twitter and LinkedIn. The information that we post on our website or on Twitter or LinkedIn could be deemed to be material information. As a result, we encourage investors, the media and others interested to review the information that we post there on a regular basis. The contents of our website or social media shall not be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended.

Scholar Rock® is a registered trademark of Scholar Rock, Inc.

Forward-Looking Statements
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding Scholar Rock’s future expectations, plans and prospects, including without limitation, Scholar Rock’s expectations regarding its growth, strategy, progress and timing of its clinical trials for apitegromab, and indication selection and development timing, including the timing of any regulatory submissions, the therapeutic potential, clinical benefits and safety of any product candidates, expectations regarding timing, success and data announcements of current ongoing preclinical and clinical trials, its cash runway, expectations regarding the achievement of important milestones, the ability of any product candidate to perform in humans in a manner consistent with earlier nonclinical, preclinical or clinical trial data, and the potential of its product candidates and proprietary platform. The use of words such as “may,” “might,” “could,” “will,” “should,” “expect,” “plan,” “anticipate,” “believe,” “estimate,” “project,” “intend,” “future,” “potential,” or “continue,” and other similar expressions are intended to identify such forward-looking statements. All such forward-looking statements are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, without limitation, whether the results from the Phase 3 SAPPHIRE trial will be sufficient to support regulatory approval, that the full results from the Phase 3 SAPPHIRE trial may differ from the topline data, that preclinical and clinical data, including the results from the Phase 2 or Phase 3 clinical trial of apitegromab, are not predictive of, may be inconsistent with, or more favorable than, data generated from future or ongoing clinical trials of the same product candidates; the data generated from Scholar Rock’s nonclinical and preclinical studies and clinical trials; information provided or decisions made by regulatory authorities; competition from third parties that are developing products for similar uses; Scholar Rock’s ability to obtain, maintain and protect its intellectual property; Scholar Rock’s dependence on third parties for development and manufacture of product candidates including, without limitation, to supply any clinical trials; and Scholar Rock’s ability to manage expenses and to obtain additional funding when needed to support its business activities and establish and maintain strategic business alliances and new business initiatives, and our ability to continue as a going concern; as well as those risks more fully discussed in the section entitled "Risk Factors" in Scholar Rock’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2024, as well as discussions of potential risks, uncertainties, and other important factors in Scholar Rock’s subsequent filings with the Securities and Exchange Commission. Any forward-looking statements represent Scholar Rock’s views only as of today and should not be relied upon as representing its views as of any subsequent date. All information in this press release is as of the date of the release, and Scholar Rock undertakes no duty to update this information unless required by law.

Scholar Rock:

Investors

Rushmie Nofsinger

Scholar Rock

rnofsinger@scholarrock.com

ir@scholarrock.com

857-259-5573

Media

Molly MacLeod

Scholar Rock

mmacleod@scholarrock.com

media@scholarrock.com

802-579-5995

Source: Scholar Rock, Inc.

FAQ

What were the key findings of SRK-439's preclinical trials for SRRK stock?

The preclinical trials showed SRK-439 combined with metformin increased lean mass by 31.6% in young mice and 10.2% in older mice, while also reducing fat mass gain compared to metformin alone.

When will Scholar Rock (SRRK) release Phase 2 EMBRAZE trial results?

Scholar Rock expects to release topline data from the Phase 2 EMBRAZE trial in the second quarter of 2025.

How does Scholar Rock's SRK-439 affect body composition in obesity treatment?

SRK-439 selectively inhibits myostatin to increase lean mass and reduce fat mass gain when combined with metformin, potentially improving body composition in obesity treatment.

Scholar Rock Holding Corporation

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