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Relay Therapeutics to Present Updated Clinical Data on RLY-2608 in HR+/HER2- Breast Cancer at 2024 San Antonio Breast Cancer Symposium

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Relay Therapeutics (RLAY) announced it will present updated clinical data for RLY-2608 in combination with fulvestrant for treating PI3Kα-mutated, HR+, HER2- locally advanced or metastatic breast cancer at the San Antonio Breast Cancer Symposium (December 10-13, 2024). The presentation, titled 'Efficacy of RLY-2608, a mutant-selective PI3Kα inhibitor in patients with PIK3CA-mutant HR+HER2- advanced breast cancer: ReDiscover trial', will be part of a poster spotlight session on targeting ER and PI3K pathway. The company will host a conference call on December 11, 2024, at 7:00 a.m. ET to discuss the findings.

Relay Therapeutics (RLAY) ha annunciato che presenterà dati clinici aggiornati per RLY-2608 in combinazione con fulvestrant, per il trattamento del cancro al seno localmente avanzato o metastatico HR+, HER2- con mutazione PI3Kα durante il San Antonio Breast Cancer Symposium (10-13 dicembre 2024). La presentazione, intitolata 'Efficacia di RLY-2608, un inibitore selettivo per mutanti di PI3Kα in pazienti con cancro al seno avanzato HR+HER2- mutato PIK3CA: trial ReDiscover', farà parte di una sessione di esposizione poster focalizzata sull'obiettivo della via ER e PI3K. L'azienda ospiterà una conferenza telefonica l'11 dicembre 2024, alle 7:00 AM ET, per discutere i risultati.

Relay Therapeutics (RLAY) anunció que presentará datos clínicos actualizados sobre RLY-2608 en combinación con fulvestrant para el tratamiento de cáncer de mama localmente avanzado o metastásico HR+, HER2- con mutación en PI3Kα en el Simposio de Cáncer de Mama de San Antonio (10-13 de diciembre de 2024). La presentación, titulada 'Eficacia de RLY-2608, un inhibidor selectivo de mutantes de PI3Kα en pacientes con cáncer de mama avanzado HR+HER2- mutado en PIK3CA: ensayo ReDiscover', formará parte de una sesión de enfoque en cartel sobre la vía ER y PI3K. La compañía realizará una conferencia telefónica el 11 de diciembre de 2024, a las 7:00 AM ET, para discutir los hallazgos.

Relay Therapeutics (RLAY)는 RLY-2608와 fulvestrant의 병용요법에 대한 최신 임상 데이터를 발표할 예정이라고 발표했습니다. 이는 PI3Kα 돌연변이, HR+, HER2- 국소 진행성 또는 전이성 유방암 치료를 위한 것입니다. 이 데이터는 2024년 12월 10일부터 13일까지 샌안토니오 유방암 심포지엄에서 발표될 예정입니다. 'PIK3CA-돌연변이 HR+HER2- 진행성 유방암 환자에서의 돌연변이 선택적 PI3Kα 억제제 RLY-2608의 효능: ReDiscover 시험'이라는 제목의 발표는 ER과 PI3K 경로를 목표로 하는 포스터 스포트라이트 세션의 일환으로 진행됩니다. 또한, 회사는 2024년 12월 11일 오전 7시 ET에 데이터에 대해 논의하기 위한 전화 회의를 개최할 예정입니다.

Relay Therapeutics (RLAY) a annoncé qu'elle présentera des données cliniques mises à jour sur RLY-2608 en combinaison avec le fulvestrant pour traiter le cancer du sein localement avancé ou métastatique HR+, HER2- avec mutation PI3Kα au San Antonio Breast Cancer Symposium (du 10 au 13 décembre 2024). La présentation, intitulée 'Efficacité de RLY-2608, un inhibiteur sélectif des mutants de PI3Kα chez les patients atteints de cancer du sein avancé HR+HER2- muté PIK3CA : essai ReDiscover', fera partie d'une session de mise en avant des affiches sur le ciblage des voies ER et PI3K. La société organisera une conférence téléphonique le 11 décembre 2024 à 7h00 ET pour discuter des résultats.

Relay Therapeutics (RLAY) kündigte an, dass aktualisierte klinische Daten zu RLY-2608 in Kombination mit Fulvestrant zur Behandlung von PI3Kα-mutiertem, HR+, HER2- lokal fortgeschrittenem oder metastasiertem Brustkrebs auf dem San Antonio Breast Cancer Symposium (10.-13. Dezember 2024) präsentiert werden. Die Präsentation mit dem Titel 'Wirksamkeit von RLY-2608, einem selektiven PI3Kα-Inhibitor bei Patienten mit PIK3CA-mutiertem HR+HER2- fortgeschrittenen Brustkrebs: ReDiscover-Studie', ist Teil einer Poster-Spotlight-Sitzung zur gezielten Behandlung der ER- und PI3K-Weg. Das Unternehmen wird am 11. Dezember 2024 um 7:00 Uhr ET eine Telefonkonferenz abhalten, um die Ergebnisse zu diskutieren.

Positive
  • Clinical trial data presentation at a major medical conference indicates progress in drug development pipeline
Negative
  • None.

Company to host conference call on Wednesday, December 11, 2024 at 7am ET

CAMBRIDGE, Mass., Dec. 09, 2024 (GLOBE NEWSWIRE) -- Relay Therapeutics, Inc. (Nasdaq: RLAY), a clinical-stage precision medicine company transforming the drug discovery process by combining leading-edge computational and experimental technologies, today announced that updated clinical data for RLY-2608 600mg BID + fulvestrant in patients with PI3Kα-mutated, HR+, HER2- locally advanced or metastatic breast cancer will be presented at the upcoming San Antonio Breast Cancer Symposium, taking place December 10-13, 2024.

Details of the RLY-2608 + fulvestrant poster presentation are as follows:
Abstract Title: PS7-01: Efficacy of RLY-2608, a mutant-selective PI3Kα inhibitor in patients with PIK3CA-mutant HR+HER2- advanced breast cancer: ReDiscover trial
Abstract Number: SESS-2211
Session: Concurrent Poster Spotlight Session 7: Targeting the ER and PI3K pathway: Novel drugs and combinations
Date/Time: Wednesday, December 11, 8:00-9:30 a.m. ET (7:00-8:30 a.m. CT)

Conference Call Information
Relay Therapeutics will host a conference call to discuss these data on Wednesday, December 11, 2024 at 7:00 a.m. ET (6:00 a.m. CT). Registration and dial-in for the conference call and webcast may be accessed through Relay Therapeutics’ website under Events in the News & Events section through the following link: https://ir.relaytx.com/news-events/events-presentations. An archived replay of the webcast will be available following the event.

The poster will be available at the start of the session on the company’s website at https://relaytx.com/publications/.

About RLY-2608

RLY-2608 is the lead program in Relay Therapeutics’ efforts to discover and develop mutant selective inhibitors of PI3Kα, the most frequently mutated kinase in all cancers, with oncogenic mutations detected in about 14% of patients with solid tumors. RLY-2608 has the potential, if approved, to address more than 300,000 patients per year in the United States, one of the largest patient populations for a precision oncology medicine.

Traditionally, the development of PI3Kα inhibitors has focused on the active, or orthosteric, site. The therapeutic index of orthosteric inhibitors is limited by the lack of clinically meaningful selectivity for mutant versus wild-type (WT) PI3Kα and off-isoform activity. Toxicity related to inhibition of WT PI3Kα and other PI3K isoforms results in sub-optimal inhibition of mutant PI3Kα with reductions in dose intensity and frequent discontinuation. The Dynamo® platform enabled the discovery of RLY-2608, the first known allosteric, pan-mutant, and isoform-selective PI3Kα inhibitor, designed to overcome these limitations. Relay Therapeutics solved the full-length cryo-EM structure of PI3Kα, performed computational long time-scale molecular dynamic simulations to elucidate conformational differences between WT and mutant PI3Kα, and leveraged these insights to support the design of RLY-2608. RLY-2608 is currently being evaluated in a first-in-human trial designed to treat patients with advanced solid tumors with a PIK3CA (PI3Kα) mutation. For more information on RLY-2608, please visit here.

About Relay Therapeutics

Relay Therapeutics is a clinical-stage precision medicine company transforming the drug discovery process by combining leading-edge computational and experimental technologies with the goal of bringing life-changing therapies to patients. As the first of a new breed of biotech created at the intersection of complementary techniques and technologies, Relay Therapeutics aims to push the boundaries of what’s possible in drug discovery. Its Dynamo® platform integrates an array of leading-edge computational and experimental approaches designed to drug protein targets that have previously been intractable or inadequately addressed. Relay Therapeutics’ initial focus is on enhancing small molecule therapeutic discovery in targeted oncology and genetic disease indications. For more information, please visit www.relaytx.com or follow us on Twitter

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, implied and express statements regarding Relay Therapeutics’ strategy, business plans and focus; the progress and timing of the clinical development of the programs across Relay Therapeutics’ portfolio; the expected therapeutic benefits and potential efficacy and tolerability of RLY-2608, both as a monotherapy and in combination with other agents, and its other programs, including lirafugratinib as well as the clinical data for RLY-2608; the interactions with regulatory authorities and any related approvals; the potential market opportunity for RLY-2608; the cash runway projection and the expectations regarding Relay Therapeutics’ use of capital, expenses and potential cost savings. The words “may,” “might,” “will,” “could,” “would,” “should,” “plan,” “anticipate,” “intend,” “believe,” “expect,” “estimate,” “seek,” “predict,” “future,” “project,” “potential,” “continue,” “target” and similar words or expressions, or the negative thereof, are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.

Any forward-looking statements in this press release are based on management's current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, risks associated with: the impact of global economic uncertainty, geopolitical instability and conflicts, or public health epidemics or outbreaks of an infectious disease on countries or regions in which Relay Therapeutics has operations or does business, as well as on the timing and anticipated results of its clinical trials, strategy, future operations and profitability; the delay or pause of any current or planned clinical trials or the development of Relay Therapeutics’ drug candidates; the risk that the preliminary or interim results of its preclinical or clinical trials may not be predictive of future or final results in connection with future clinical trials of its product candidates and that interim and early clinical data may change as more patient data become available and are subject to audit and verification procedures; Relay Therapeutics’ ability to successfully demonstrate the safety and efficacy of its drug candidates; the timing and outcome of its planned interactions with regulatory authorities; and obtaining, maintaining and protecting its intellectual property. These and other risks and uncertainties are described in greater detail in the section entitled “Risk Factors” in Relay Therapeutics’ most recent Annual Report on Form 10-K and Quarterly Report on Form 10-Q, as well as any subsequent filings with the Securities and Exchange Commission. In addition, any forward-looking statements represent Relay Therapeutics' views only as of today and should not be relied upon as representing its views as of any subsequent date. Relay Therapeutics explicitly disclaims any obligation to update any forward-looking statements. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.

Contact:
Megan Goulart
617-322-0814
mgoulart@relaytx.com

Media:
Dan Budwick
1AB
973-271-6085
dan@1abmedia.com


FAQ

What is RLY-2608 and what type of cancer is it targeting?

RLY-2608 is a mutant-selective PI3Kα inhibitor being developed for PI3Kα-mutated, HR+, HER2- locally advanced or metastatic breast cancer, studied in combination with fulvestrant.

When will Relay Therapeutics (RLAY) present the RLY-2608 clinical data?

Relay Therapeutics will present the RLY-2608 clinical data on December 11, 2024, during the San Antonio Breast Cancer Symposium, with a company conference call scheduled for 7:00 a.m. ET the same day.

What is the name of the clinical trial for RLY-2608?

The clinical trial for RLY-2608 is called the ReDiscover trial, studying its efficacy in PIK3CA-mutant HR+HER2- advanced breast cancer.

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