Allogene Therapeutics (ALLO) Q1 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q1 2026 earnings summary
20 May, 2026Executive summary
Interim analysis from the pivotal Phase 2 ALPHA3 trial showed cema-cel achieved a 58.3% MRD clearance rate in first-line LBCL, outperforming observation by 41.6 percentage points and demonstrating a favorable safety profile with no CRS, ICANS, GvHD, or treatment-related hospitalizations, supporting outpatient use and broader accessibility, including community cancer centers.
ALLO-329 in autoimmune indications is progressing through dose escalation in the RESOLUTION trial, with early clinical activity and favorable tolerability at lower doses.
Pipeline prioritization centers on ALPHA3 (cema-cel for LBCL), RESOLUTION (ALLO-329 for autoimmune diseases), and TRAVERSE (ALLO-316 for RCC), with ALLO-316 Phase 1b expansion cohort completed.
Company completed a $200.4 million public offering in April 2026, extending cash runway into Q1 2029.
Community and global clinical sites show strong interest in outpatient administration and broader accessibility for both lead programs.
Financial highlights
Q1 2026 net loss was $42.6 million, or $0.18 per share, compared to $59.7 million, or $0.28 per share, in Q1 2025.
Research and development expenses were $32.0 million; general and administrative expenses were $14.1 million.
Cash, cash equivalents, and investments totaled $266.9 million as of March 31, 2026, before the April 2026 offering.
April 2026 public offering raised $200.4 million gross ($187.9 million net), extending cash runway into Q1 2029.
Stockholders’ equity was $278.9 million as of March 31, 2026.
Outlook and guidance
Cash runway, including April 2026 offering proceeds, is expected to fund operations through completion of ALPHA3 and phase I RESOLUTION study for ALLO-329, with key data updates in Q4 2026 and interim EFS analysis for ALPHA3 in mid-2027, and primary EFS analysis in mid-2028.
Operating cash expense guidance for 2026 increased to $150–$165 million; GAAP operating expenses expected at $210–$225 million, including $35 million in non-cash stock-based compensation.
Latest events from Allogene Therapeutics
- ALPHA3 study shows strong MRD clearance and safety, with major catalysts and cash runway to 2029.ALLO
Jefferies Global Healthcare Conference 20263 Jun 2026 - Zachary Roberts appointed CEO and director, with updated compensation; voting process unchanged.ALLO
Proxy filing28 May 2026 - Executive compensation totals corrected; no changes to voting matters or proposals.ALLO
Proxy filing21 May 2026 - Pivotal CAR T programs show strong efficacy, safety, and broad market potential.ALLO
Corporate presentation18 May 2026 - Pivotal trials advance, key data in 2026, cash runway into Q1 2028, net loss narrowed.ALLO
Q4 20253 May 2026 - Annual meeting to address director elections, executive pay, share increase, and auditor ratification.ALLO
Proxy filing1 May 2026 - Key votes include director elections, doubling authorized shares, and auditor ratification.ALLO
Proxy filing30 Apr 2026 - Key votes include director elections, executive pay, share increase, and auditor ratification.ALLO
Proxy filing20 Apr 2026 - Cema-cel achieved 58.3% MRD clearance and strong safety, supporting outpatient use in LBCL.ALLO
Study result20 Apr 2026