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Mar 31, 2022

Beam Therapeutics Q1 2022 Earnings Report

Announced pipeline and business highlights and reported financial results.

Key Takeaways

Beam Therapeutics reported its Q1 2022 financial results, highlighting advancements in its pipeline, including progress with BEAM-101, BEAM-102, and BEAM-201 programs, and the initiation of IND-enabling studies for BEAM-301. The company ended the quarter with $1.2 billion in cash, cash equivalents, and marketable securities.

BEAM-101 patient enrollment, BEAM-102 and BEAM-201 IND submissions and BEAM-301 IND-Enabling Studies are all on-track for the second half of 2022

A Natural History Study was initiated in people with Sickle Trait to provide insights into key characteristics of Sickle Cell Trait and Sickle Cell Disease

Manmohan Singh, Ph.D., was appointed to Executive Leadership Team and Anne Marie Woodland was appointed as Head of Regulatory

Ended First Quarter 2022 with $1.2 Billion in Cash, Cash Equivalents and Marketable Securities

Total Revenue
$8.43M
Previous year: $6K
+140433.3%
EPS
-$1.01
Previous year: -$3.35
-69.9%
Gross Profit
$3.17M
Previous year: -$190M
-101.7%
Cash and Equivalents
$1.22B
Previous year: $503M
+142.8%
Free Cash Flow
$211M
Previous year: -$50.1M
-522.0%
Total Assets
$1.45B
Previous year: $693M
+109.7%

Beam Therapeutics

Beam Therapeutics

Forward Guidance

The press release contains forward-looking statements regarding the AUNT Study, presentations at ASGCT, nomination of additional development candidates, initiation of IND-enabling studies and submission of IND applications, the therapeutic applications and potential of Beam's technology, the planned initiation and design of the BEACON-101 clinical trial, the sufficiency of capital resources, and the ability to develop life-long, curative, precision genetic medicines.

Positive Outlook

  • Intended design and planned initiation of the AUNT Study
  • Plans and anticipated timing to nominate additional development candidates
  • Plans and anticipated timing to initiate IND-enabling studies
  • Plans and anticipated timing to submit IND applications
  • Ability to develop life-long, curative, precision genetic medicines for patients through base editing

Challenges Ahead

  • Ability to develop, obtain regulatory approval for, and commercialize product candidates may take longer or cost more than planned
  • Ability to raise additional funding may not be available
  • Ability to obtain, maintain and enforce patent and other intellectual property protection for product candidates
  • Preclinical testing and preliminary data from studies and trials may not be predictive of results
  • Enrollment of clinical trials may take longer than expected