NANOBIOTIX Provides Third Quarter 2022 Operational and Financial Update
- Established recommended Phase 2 dose (RP2D) for NBTXR3 plus anti-PD-1 in patients with locoregional recurrent and recurrent and/or metastatic head and neck cancer, lung metastases from any primary tumor, or liver metastases from any primary tumor
- Updated Phase 1 NBTXR3 plus anti-PD-1 safety and efficacy data in recurrent and/or metastatic advanced cancers from Study 1100 to be presented at SITC 2022 on
November 10 th - Bolstered NBTXR3 strategic development capability with the appointment of twelve global medical experts to the
Nanobiotix Scientific Advisory Board - €53.5 million in cash and cash equivalents extends cash runway into Q1 2024
“This quarter saw us continue our prioritized focus on the advancement of NBTXR3 both as a single agent activated by radiotherapy and as a combination therapy with anti-PD-1 for patients with locally advanced head and cancer and recurrent and/or metastatic head and neck cancer, respectively,” said
Third Quarter Financial Updates
In
Third Quarter Operational Highlights and Expected Upcoming Milestones
Bolstered NBTXR3 strategic development capability with appointment of global medical experts to the
- Board includes twelve (12) leading radiation, medical and surgical oncologists from the United States and
Europe with expertise across the fundamental disciplines responsible for decision-making in oncology that will support the development of lead therapeutic candidate NBTXR3
Priority Registration Pathway in Locally Advanced Head & Neck Squamous Cell Carcinoma (LA-HNSCC), Local Control as Single Agent Activated by Radiotherapy (RT):
- NANORAY-312 Phase 3 trial evaluating RT-activated NBTXR3 ± cetuximab in elderly patients with LA-HNSCC
- Strategic partner
LianBio enrolled the first patient inAsia - Initiated clinical site activation in
the United States (US) - Ongoing ramp up by
LianBio of regional site activations inAsia - Expect patient enrollment in the US to begin in Q4 2022
- Strategic partner
- Study 102 Phase 1 trial evaluating RT-activated NBTXR3 in LA-HNSCC
- Interim update in
February 2022 reported ongoing median overall survival of 17.9 months in the all-treated population (n=56) and 23.0 months in evaluable patients (n=44) - Additional safety and efficacy data from full study population with minimum follow-up of one year expected in mid-2023
- Interim update in
Priority Pathway in Immunotherapy for Recurrent/Metastatic Head & Neck Squamous Cell Carcinoma (R/M HNSCC), Priming Immune Response in Combination with Anti-PD-1 Treatment:
- Study 1100 Phase 1 dose escalation and expansion trial evaluating RT-activated NBTXR3 in combination with an anti-PD-1 in patients with advanced cancers
- Completed enrollment for dose escalation and initiated dose expansion phase of the study
- Determined recommended Phase 2 dose (RP2D) that will serve as the proposed dose for planned registration pathway in patients with inoperable R/M HNSCC that is resistant to prior immunotherapy
- Poster presentation highlighting dose escalation data to be presented at the
Society for Immunotherapy of Cancer (SITC) annual conference and details of these findings to be reviewed during the Company’s scheduled third quarter conference call onThursday, November 10 th
- Phase 3 registrational program for patients with unresectable locoregional recurrent (LRR) or relapsed or metastatic HNSCC resistant to previous anti-PD-1/PD-L1 therapy
- Protocol submission to
US FDA for potential registration pathway for NBTXR3 in combination with immunotherapy in R/M HNSCC expected by Q1 2023
- Protocol submission to
Expanding NBTXR3 Opportunity, Collaborating with
- Ongoing collaboration with
The University of Texas MD Anderson Cancer Center - Determination of RP2D for NBTXR3 in pancreatic ductal adenocarcinoma (PDAC) expected by year-end 2022
- Initial Phase 1b/2 data for NBTXR3 in patients with non-small cell lung cancer (NSCLC), esophageal cancer and PDAC expected in 2023
Conference Call and Webcast
A live webcast of the call may be accessed by visiting the investors section of the company’s website at www.nanobiotix.com. Participants may register for the call here. They will be able to join the call via dial-in or one-click dial-out. It is recommended to join 10 minutes prior the event start.
Participants are invited to email their questions in advance to investors@nanobiotix.com.
A replay of the webcast will be available shortly after the conclusion of the call and will be archived on the company's website.
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This press release contains certain “forward-looking” statements within the meaning of applicable securities laws, including the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by words such as “at this time,” “anticipate,” “believe,” “can,” “could,” “estimate,” “expect,” “intend,” “is designated to,” “may,” “might,” “on track,” “plan,” “potential,” “predict,” “objective,” “shall,” “should,” “scheduled,” and “will,” or the negative of these and similar expressions. These forward-looking statements, which are based on our management’s current expectations and assumptions and on information currently available to management, include statements about the timing and progress of clinical trials, the timing of our presentation of data, the results of our preclinical and clinical studies and their potential implications. Such forward-looking statements are made in light of information currently available to us and based on assumptions that
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Investor Relations Department SVP, Investor Relations +1 (609) 678-7388 investors@nanobiotix.com |
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Source: Nanobiotix S.A.