- JDQ443, an investigational selective, covalent, and orally bioavailable KRASG12C inhibitor, shows 57% confirmed ORR at recommended dose of 200 mg twice daily in Phase Ib study in patients with advanced non-small cell lung cancer (NSCLC)
- Ongoing investigation of JDQ443 in single agent and multiple combination strategies designed to enhance efficacy of G12C targeted therapy and improve outcomes of patients with KRAS G12C-driven cancers. Phase III study anticipated to begin mid 2022
- Innovation in targeted protein degradation also highlighted with debut for protein degrader DKY709, an investigational molecular glue
Basel, April 11, 2022 — Novartis today announced promising clinical data for JDQ443, an investigational selective, covalent, and orally bioavailable KRASG12C inhibitor at the annual meeting of American Association for Cancer Research (AACR). Comprehensive information on the discovery of JDQ443 is also included in a poster being presented on Wednesday 13th April with further details published in the journal Cancer Discovery1.
Preliminary data (Phase Ib) from the KontRASt-01 study (NCT04699188) showed that JDQ443, discovered at Novartis, demonstrated anti-tumor activity, high systemic exposure at its recommended dose, and a favorable safety profile based on initial clinical data in patients with KRAS G12C-mutated solid tumors2. The data were submitted as a late-breaking abstract and will be presented today in an oral session.
KRAS mutations are the most frequent oncogenic drivers in NSCLC, the most common type of lung cancer3. The most common form of KRAS mutation is G12C4. JDQ443 inhibits this mutated form of KRAS in a structurally distinct way, trapping KRAS G12C in a GDP-bound, inactive state while avoiding direct interaction with H95, a recognized route for resistance5,6. In preclinical models, JDQ443 potently inhibited KRAS G12C cellular signalling and proliferation in a mutant-selective manner and demonstrated dose-dependent antitumor activity7.
“After decades without a breakthrough, we as an industry are entering a transformative era in targeted treatment for KRAS-mutated cancers,” said Jeff Legos, Executive Vice President, Global Head of Oncology & Hematology Development at Novartis. “But challenges remain, in particular drug resistance. We believe that JDQ443 may have the potential for overcoming such challenges. Today’s preliminary data are an encouraging signal that we are on the right path as we continue to investigate single-agent and multiple combination strategies designed to enhance efficacy of G12C targeted therapy and improve outcomes of patients with KRAS G12C-driven cancers.”
Also at AACR, Novartis debuted its targeted protein degradation platform with presentations on DKY709, a potential first-in-class “molecular glue” protein degrader that is designed to target the zinc finger transcription factor Helios (IKZF2)8. Transcription factors, similar to KRAS G12C, are historically "undruggable" targets. Clinical data were drawn from a study (NCT03891953) of advanced solid tumors in which DKY709 is being investigated as a monotherapy and in combination with the anti–PD-1 antibody spartalizumab. The discovery and structure of DKY709 were also presented on April 9th at AACR9.
About JDQ443 and the KontRASt-01 Study2
KontRASt-01 (NCT04699188) is a phase Ib/II open-label, multi-center, dose escalation study of JDQ443, in patients with advanced solid tumors harboring the KRAS G12C mutation, including NSCLC and colorectal cancer. The study began in February 2021 and is currently recruiting. The escalation part will further characterize the safety and tolerability profile of JDQ443 as a single agent and JDQ443 in combination with other agents in advanced solid tumor patients. The estimated primary completion date of the study is 2024.
The preliminary data presented at AACR were drawn from the monotherapy dose escalation arm of the KontRASt-01 study. Patients had a median of 3 prior lines of anti-neoplastic therapy. The recommended monotherapy dose of 200 mg taken orally twice daily (BID) will be taken forward for further studies in phase II dose expansion. Efficacy data (cutoff of 05 Jan 2022) from the pooled Phase Ib JDQ443 single agent cohort (n=39) showed:
- 57% (4/7) confirmed overall response rate (ORR) at 200 mg BID in NSCLC
- 45% (9/20) confirmed and unconfirmed ORR across doses in NSCLC
- 35% (7/20) confirmed ORR across doses in NSCLC
- PD/PK modeling predicts sustained, high-level target occupancy at the recommended dose of 200 mg BID
Ongoing enrollment to the KontRASt-01 study continues across a number of arms:
- JDQ443 single agent expansion (Ph II) in KRAS G12C-mutated NSCLC
- JDQ443 single agent expansion (Ph II) in KRAS G12C-mutated CRC
- JDQ443 + TNO155 (SHP2 inhibitor) dose escalation (Ph Ib) in KRAS G12C-mutated solid tumors
- JDQ443 + tislelizumab dose escalation (Ph Ib) in KRAS G12C-mutated solid tumors
A Phase III study, KontRASt-02 (NCT05132075) of JDQ443 versus docetaxel in patients with previously treated, locally advanced or metastatic KRAS G12C-mutated NSCLC is anticipated to begin enrolling patients by mid-2022.
Novartis in Lung Cancer
The needs in lung cancer are urgent and significant. Each year, more than 2 million people are newly diagnosed globally10, and lung cancer remains the number one cause of cancer-related death worldwide11.There are two main types of lung cancer—small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). NSCLC accounts for approximately 85% of lung cancer diagnoses12.
Novartis is making bold investments in advancing the science to research treatments that may make an impact for patients around the world. The company is committed to working with the scientific and medical communities to reimagine the treatment of lung cancer and pursue advances in medicine that could extend the survival of people living with lung cancer.
With one of the most diverse lung cancer development programs in the industry, Novartis is developing therapies that may block cancer growth and activate the body’s immune system; working to understand the relationship between chronic inflammation and tumor growth and progression; and exploring the potential for advanced nuclear medicine to fight the disease. Through these programs, Novartis aims to redefine possibilities in lung cancer and pursue a trajectory to make lung cancer history.
Targeted Protein Degradation at Novartis
Targeted protein degradation (TPD) offers first-in-class potential for multiple previously undruggable targets. The approach induces proximity of a target to a ubiquitin ligase, thereby tagging the target for destruction by the cell. Novartis is making an enterprise scale investment in TPD innovation, focusing on the discovery of molecular glues and bifunctional degraders, as well as the development of chemical libraries and the discovery of structural insights.
This media update contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements can generally be identified by words such as “potential,” “can,” “will,” “plan,” “may,” “could,” “would,” “expect,” “anticipate,” “look forward,” “believe,” “committed,” “investigational,” “pipeline,” “launch,” or similar terms, or by express or implied discussions regarding potential marketing approvals, new indications or labeling for the investigational or approved products described in this media update, or regarding potential future revenues from such products. You should not place undue reliance on these statements. Such forward-looking statements are based on our current beliefs and expectations regarding future events, and are subject to significant known and unknown risks and uncertainties. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the forward-looking statements. There can be no guarantee that the investigational or approved products described in this media update will be submitted or approved for sale or for any additional indications or labeling in any market, or at any particular time. Nor can there be any guarantee that such products will be commercially successful in the future. In particular, our expectations regarding such products could be affected by, among other things, the uncertainties inherent in research and development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement pressures and requirements for increased pricing transparency; our ability to obtain or maintain proprietary intellectual property protection; the particular prescribing preferences of physicians and patients; general political, economic and business conditions, including the effects of and efforts to mitigate pandemic diseases such as COVID-19; safety, quality, data integrity or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred to in Novartis AG’s current Form 20-F on file with the US Securities and Exchange Commission. Novartis is providing the information in this media update as of this date and does not undertake any obligation to update any forward-looking statements contained in this media update as a result of new information, future events or otherwise.
Novartis is reimagining medicine to improve and extend people’s lives. As a leading global medicines company, we use innovative science and digital technologies to create transformative treatments in areas of great medical need. In our quest to find new medicines, we consistently rank among the world’s top companies investing in research and development. Novartis products reach nearly 800 million people globally and we are finding innovative ways to expand access to our latest treatments. About 108,000 people of more than 140 nationalities work at Novartis around the world. Find out more at https://www.novartis.com.
Novartis is on Twitter. Sign up to follow @Novartis at https://twitter.com/novartisnews
For Novartis multimedia content, please visit https://www.novartis.com/news/media-library
For questions about the site or required registration, please contact [email protected]
- Weiss A, Lorthiois E, Barys L, et al. Discovery, Preclinical Characterization, and Early Clinical Activity of JDQ443, a Structurally Novel, Potent and Selective, Covalent Oral Inhibitor of KRASG12CCancer Discovery 2022
- Tan D, Shimizu T, Solomon B, et al. KontRASt-01: A Phase Ib/II, dose-escalation study of JDQ443 in patients with advanced, KRAS G12C-mutated solid tumors. AACR 2022.
- Skoulidis F & Heymach JV. Nat Rev Cancer 2019;19:495–509.
- Arbour KC, et al. Clin Cancer Res 2018;24:334–340.
- Cotesta S et al. EFMC-ISMC 2021; Poster LE054
- Awad MM, et al. New Engl J Med 2021;384:2382–2392
- Brachmann SM et al. AACR-NCI-EORTC 2021
- D’Hennezel, E. Characterization of a first-in-class molecular glue degrader to modulate T cell activity in cancer. AACR 2022.
- Bonazzi, S. Discovery of a first-in-class molecular glue degrader for immuno-oncology indications. AACR 2022.
- Ferlay J, Ervik M, Lam F, et al. Global Cancer Observatory: Cancer Today. Lyon: International Agency for Research on Cancer; 2020 (https://gco.iarc.fr/today, accessed March 2022).
- Lemjabbar-Alaoui H, Hassan OU, Yang Y-W, et al. Lung cancer: biology and treatment options. Biochim Biophys Acta. 2015. 1856(2):189-210.
- WHO above + American Cancer Society. About Lung Cancer. Available at https://www.cancer.org/cancer/non-small-cell-lung-cancer/about/what-is-non-small-cell-lung-cancer.html. Accessed September 10, 2021.
# # #
Novartis Media Relations
E-mail: [email protected]
| Anja von Treskow|
Novartis External Communications
+41 79 939 28697 (mobile)
Novartis US External Communications
+1 862 579 8456
| Mary Carmichael|
+1 617 413 3543 (mobile)
Novartis Investor Relations
Central investor relations line: +41 61 324 7944
E-mail: [email protected]
|Samir Shah||+41 61 324 7944||Sloan Simpson||+1 862 345 4440|
|Nicole Zinsli-Somm||+41 61 324 3809||Alina Levchuk||+1 862 778 3372|
|Isabella Zinck||+41 61 324 7188||Parag Mahanti||+1 973-876-4912|