Adaptive Biotechnologies Stock Price, News & Analysis

Adaptive Biotechnologies (Nasdaq: ADPT), a commercial stage biotechnology company focused on adaptive immune system genetics and clinical products, has announced its participation in the 43rd Annual J.P. Morgan Healthcare Conference in San Francisco.

The company's management will deliver their presentation on Tuesday, January 14th at 5:15 p.m. Pacific Time / 8:15 p.m. Eastern Time. Investors and interested parties can access both live and archived versions of the presentation through the 'Investors' section on the company's website at www.adaptivebiotech.com.

Adaptive Biotechnologies (ADPT) presented new data at the 66th ASH Annual Meeting showcasing the effectiveness of their clonoSEQ® test in measuring residual disease (MRD) for blood cancer treatment. Key findings from multiple studies demonstrate that achieving MRD levels below 10⁻⁶ correlates with improved patient outcomes.

The Phase 3 ECOG-ACRIN EA4151 trial revealed that mantle cell lymphoma patients with undetectable MRD may not need autologous transplantation. The FELIX study showed 84% of treatment responders achieved MRD <10⁻⁶, associated with better survival rates. Additional studies in multiple myeloma, chronic lymphocytic leukemia, and pediatric B-ALL further validated clonoSEQ's utility in guiding treatment decisions and monitoring disease progression.

Adaptive Biotechnologies (Nasdaq: ADPT) announced that its clonoSEQ® test for measurable residual disease (MRD) assessment will be featured in over 65 abstracts at the 66th ASH Annual Meeting. The presentations span eight different types of blood cancer and include a plenary session, a late-breaking abstract, and 25 oral presentations. The studies demonstrate clonoSEQ's role as a standard for efficacy measurement in pivotal clinical trials and highlight its advantages in both clinical trials and real-world practice. Several practice-changing studies use MRD as a primary endpoint in multiple myeloma, mantle cell lymphoma, and chronic lymphocytic leukemia.

Adaptive Biotechnologies reported its Q3 2024 financial results, highlighting a 22% revenue increase to $46.4 million compared to Q3 2023. The MRD business contributed 81% of revenue, growing 52% year-over-year, with clonoSEQ test volume rising 30% to 19,600 tests. The company achieved an updated Medicare CLFS Gapfill rate for clonoSEQ at $2,007 per test, a 17% increase, and expanded Medicare coverage for Mantle Cell Lymphoma.

Operating expenses decreased 11% to $79.1 million, with a net loss of $32.1 million, down from $50.3 million in Q3 2023. Adjusted EBITDA loss improved to $14.3 million from $29.8 million. Cash reserves stood at $267.2 million.

Updated 2024 guidance projects MRD revenue between $143 million and $145 million and total operating expenses between $335 million and $340 million.

Adaptive Biotechnologies (NASDAQ: ADPT) announced expanded Medicare coverage for its clonoSEQ test to include measurable residual disease (MRD) assessment in mantle cell lymphoma (MCL) patients. The coverage follows Medicare's episode pricing structure with an updated rate of $8,029. MCL, affecting approximately 4,000 new cases annually in the US, is an aggressive form of non-Hodgkin lymphoma where most patients experience multiple relapses. clonoSEQ offers a minimally invasive, blood-based MRD testing option to assess treatment response and monitor disease progression. This expansion adds to existing Medicare coverage for multiple myeloma, chronic lymphocytic leukemia, B-cell acute lymphoblastic leukemia, and diffuse large B-cell lymphoma.

Adaptive Biotechnologies (Nasdaq: ADPT), a commercial stage biotechnology company focused on translating adaptive immune system genetics into clinical products for disease diagnosis and treatment, has announced its third quarter 2024 financial results release date. The company will report its financial results on Thursday, November 7, 2024, after the market closes.

Following the release, Adaptive Biotechnologies will host a conference call and webcast at 1:30 p.m. Pacific Time / 4:30 p.m. Eastern Time on the same day. Investors can access the live audio webcast through the 'Investors' section of the company's website at www.adaptivebiotech.com. For those unable to attend live, an archived version of the webcast will be made available within 24 hours after the event.

Adaptive Biotechnologies (Nasdaq: ADPT) has announced that its clonoSEQ® test has received In Vitro Diagnostic Regulation (IVDR) 2017/746 Class C certification in the European Union. This makes clonoSEQ the first IVDR-certified test for detecting minimal residual disease (MRD) in patients with lymphoid malignancies. The certification allows for broad use in assessing MRD status and changes in disease burden for B-cell malignancies.

clonoSEQ is widely adopted in patient care and clinical trials, with over 3,700 clinicians using it clinically in the past year and its inclusion in more than 160 active biopharma-sponsored trials. The test is available in several European countries through technology transfer partnerships with major academic laboratories, with additional partnerships expected later in 2024.

Adaptive Biotechnologies (Nasdaq: ADPT), a commercial stage biotechnology company, has announced its participation in the Morgan Stanley 22nd Annual Global Healthcare Conference in New York, NY. The company's management will take part in a fireside chat on Friday, September 6th at 9:20 a.m. Pacific Time / 12:20 p.m. Eastern Time.

Adaptive Biotechnologies focuses on translating the genetics of the adaptive immune system into clinical products for disease diagnosis and treatment. Interested parties can access a live and archived webcast of the presentation through the 'Investors' section of the company's website at www.adaptivebiotech.com.

Adaptive Biotechnologies (Nasdaq: ADPT) reported Q2 2024 financial results, showing a 12% decrease in total revenue to $43.2 million. However, the MRD business grew 36% to $35.3 million, contributing 82% of total revenue. clonoSEQ test volume increased 36% to 18,520 tests. Operating expenses decreased 6% to $90.5 million, including $7.2 million in long-lived assets impairment charges. Net loss was $46.2 million, slightly improved from $47.8 million in Q2 2023. The company updated its 2024 guidance, raising the MRD revenue range to $140-$145 million and reducing expected operating expenses to $340-$350 million. Cash, cash equivalents, and marketable securities stood at $291.9 million as of June 30, 2024.