Welcome to our dedicated page for Allogene Therapeutics news (Ticker: ALLO), a resource for investors and traders seeking the latest updates and insights on Allogene Therapeutics stock.
Allogene Therapeutics, Inc. (ALLO) is a clinical-stage biotechnology leader developing off-the-shelf CAR T cell therapies for cancer and autoimmune diseases. This news hub provides investors and industry professionals with timely updates on clinical advancements, regulatory milestones, and strategic partnerships shaping the future of allogeneic cell treatments.
Access authoritative updates on ALLO's innovative pipeline, including progress with Dagger® technology and CRISPR-engineered therapies. Our curated news collection offers:
- Press releases detailing trial results and FDA interactions
- Financial reports and earnings call summaries
- Analysis of collaborations with academic and industry partners
- Updates on manufacturing scalability and therapeutic applications
Bookmark this page for centralized access to verified information on Allogene's progress in creating accessible, next-generation cell therapies. Check regularly for developments in hematologic malignancies, solid tumor treatments, and autoimmune disease research.
Allogene Therapeutics announced that the FDA granted Regenerative Medicine Advanced Therapy (RMAT) designation to ALLO-316 for treating adult patients with CD70 positive advanced or metastatic renal cell carcinoma (RCC). The designation was based on clinical data from the TRAVERSE trial, showing potential in treating patients who failed multiple standard RCC therapies. ALLO-316 utilizes the Dagger® technology as a next-generation allogeneic platform for single-infusion 'off-the-shelf' CAR T therapy. The company will present updated Phase 1 data at the upcoming SITC annual meeting. ALLO-316 previously received Fast Track Designation in March 2022.
Allogene Therapeutics, Inc. (Nasdaq: ALLO), a clinical-stage biotechnology company focused on developing allogeneic CAR T (AlloCAR T™) products for cancer and autoimmune disease, has announced its participation in the Goldman Sachs Cell Therapy Day Conference. The event is scheduled for October 1, 2024 in New York.
Allogene will be part of a panel discussion centered on innovations in the allogeneic cell therapy landscape. The panel is set to take place at 10:00 AM PT/1:00 PM ET. A webcast of the discussion will be available on the company's website at www.allogene.com under the Investors tab in the News and Events section. The replay will remain accessible for approximately 30 days after the live webcast.
Allogene Therapeutics (Nasdaq: ALLO) will present pre-clinical data for ALLO-329, its next-generation investigational AlloCAR T candidate for autoimmune indications, at the ACR Convergence 2024. ALLO-329 is a CD19/CD70 dual AlloCAR T product designed to target both B-cells and T-cells implicated in autoimmune diseases. It utilizes CRISPR-based site-specific integration and incorporates the Dagger® technology to potentially reduce or eliminate the need for lymphodepletion.
The company aims to address challenges in CAR T therapy for autoimmune diseases by making it available off-the-shelf and potentially reducing chemotherapy conditioning. Allogene plans to file an IND application in Q1 2025 and expects proof-of-concept by year-end 2025.
Allogene Therapeutics (Nasdaq: ALLO), a clinical-stage biotechnology company focused on developing allogeneic CAR T (AlloCAR T™) products for cancer and autoimmune diseases, has announced its participation in two upcoming investor conferences:
1. Canaccord Genuity 44th Annual Growth Conference on Tuesday, August 13, 2024, at 7:00 AM PT/10:00 AM ET
2. Baird 2024 Global Healthcare Conference on Wednesday, September 11, 2024, at 7:15 AM PT/10:15 AM ET
Webcasts, if available, will be accessible on the company's website at www.allogene.com under the Investors tab in the News and Events section. Replays will be available for approximately 30 days after the live webcasts.
Allogene Therapeutics reported Q2 2024 financial results and provided business updates. Key highlights include:
1. Initiation of pivotal Phase 2 ALPHA3 trial for cema-cel in 1L LBCL consolidation, with enrollment completion expected in 1H 2026 and potential BLA submission in 2027.
2. ALLO-329 IND application for autoimmune diseases on track for Q1 2025, with proof-of-concept data expected by YE 2025.
3. ALLO-316 Phase 1 TRAVERSE data update in RCC planned for YE 2024.
4. Q2 2024 ended with $444.6M in cash, cash equivalents, and investments, with runway projected into 2H 2026.
5. Q2 2024 net loss of $66.4M, or $0.35 per share.
6. 2024 guidance unchanged, expecting a decrease in cash of ~$200M and GAAP Operating Expenses of ~$300M.
Allogene Therapeutics (Nasdaq: ALLO), a clinical-stage biotechnology company focused on developing allogeneic CAR T (AlloCAR T™) products for cancer and autoimmune diseases, has announced its plans to report second quarter 2024 financial results and provide a business update. The company will host a conference call and webcast on August 7, 2024, at 2:00 p.m. PT/5:00 p.m. ET, following the market close.
Investors and interested parties can access the listen-only webcast on Allogene's website under the Investors tab in the News and Events section. A replay will be available for approximately 30 days. Those wishing to participate in the Q&A session during the conference call must register separately to receive a personal PIN for access.
Allogene Therapeutics (Nasdaq: ALLO) has activated three community cancer centers for its pivotal Phase 2 ALPHA3 trial of cemacabtagene ansegedleucel (cema-cel) for large B-cell lymphoma (LBCL). The trial aims to improve 1L cure rates for patients with minimal residual disease (MRD). The centers include Rocky Mountain Cancer Centers, Astera Cancer Care, and Norton Cancer Institute. Detection of MRD will use the Foresight CLARITY IUO MRD test, powered by PhasED-Seq. Enrollment is expected to complete by 1H 2026, with a potential BLA submission in 2027. The trial could expand access to CAR T therapies in community settings, where 80% of patients are treated.
Community-based practices are first to enroll in ALPHA3, signaling a move to broader CAR T adoption. This trial addresses two key questions: can circulating tumor DNA predict relapse, and does cema-cel improve cure rates compared to conventional methods? With over 19 locations in Colorado, RMCC provides comprehensive cancer care. ACC, part of OneOncology, serves over 22,000 patients annually through 13 locations. Norton Cancer Institute, with 21 locations, treats over 4,000 new patients yearly.
Allogene Therapeutics has initiated the pivotal Phase 2 ALPHA3 trial to evaluate cemacabtagene ansegedleucel (cema-cel) as part of the first-line treatment for large B-cell lymphoma (LBCL) patients likely to relapse. The trial aims to improve cure rates by using Foresight Diagnostics' CLARITY™ test to identify patients with minimal residual disease (MRD) who need further treatment. Enrollment is expected to be completed in the first half of 2026, with a Biologics License Application (BLA) submission anticipated in 2027. The trial will enroll approximately 240 patients and will assess the efficacy of cema-cel in improving event-free survival (EFS) compared to the current standard of care.
Allogene Therapeutics (Nasdaq: ALLO), a clinical-stage biotech company specializing in allogeneic CAR T (AlloCAR T™) products for cancer and autoimmune diseases, will participate in the TD Cowen 5th Annual Oncology Innovation Summit.
The event is scheduled for May 28, 2024, at 9:30 am PT/12:30 pm ET. A webcast will be available on the company's website under the Investors section. Replays of the webcast will be accessible for approximately 30 days.
Allogene Therapeutics (Nasdaq: ALLO), a clinical-stage biotech firm, announced a $110 million common stock offering, pricing 37,931,035 shares at $2.90 each. The offering, backed by mutual funds, institutional investors, and the company's board and executives, is expected to close by May 16, 2024. Managed by Goldman Sachs, the offering is under a shelf registration statement filed in March and declared effective by the SEC in April 2024. The proceeds will be used for continued development of their AlloCAR T™ products for cancer and autoimmune diseases.