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北京时间·🕒 发布 19:35:27(美东 07:35)·⟳ 抓取 19:35:36 +9s·⚡ 决策 07-30 19:46:14 +10m38s·89.0 天前

Crescent Biopharma披露二季度财务结果,现金可支持运营至2028年下半年

本次公告主要是例行季度财务披露,未包含新的临床数据、监管里程碑、授权交易或可量化商业化增量。

📄 原文CBIO↗ 原文
Crescent Biopharma Reports Second Quarter 2026 Financial Results and Recent Business Highlights
Second Quarter 2026 Financial Results Cash position: Cash and cash equivalents were $171.6 million as of June 30, 2026.…
不做 Crescent Biopharma(CBIO.US)
例行季度财务披露,现金 runway 与亏损数据不足以形成短线正期望;没有新的临床、监管、订单或授权交易催化,不做。
展开详情(成交明细 / 研究档案 / 原文全文 / 决策记录链)

研究档案

🔎 新鲜度:最早出现 2026-07-30 · 扩散 low · price-in 风险 medium ↗

关键理由

  • 本次公告主要是例行季度财务披露,未包含新的临床数据、监管里程碑、授权交易或可量化商业化增量。
  • 公司披露二季度净亏损2480万美元、研发费用上升及融资后现金3.051亿美元,但这些更像现金 runway 更新而非短线重定价催化。

主要风险

  • 7月公开发行带来的摊薄已在公告中列示,但作为融资后现金 runway 的配套信息,缺少新的公司级净损害事实。

原文全文

展开原文 · 8,518 字
Second Quarter 2026 Financial Results
Cash position:
Cash and cash equivalents were $171.6 million as of June 30, 2026. Pro forma cash was $305.1 million as of June 30, 2026, reflecting an additional $133.5 million in net proceeds from the July 2026 public offering. Crescent expects that its existing cash and cash equivalents will fund operations into the second half of 2028.
Research and development (R&D) expenses:
R&D expenses were $19.4 million and $12.1 million for the three months ended June 30, 2026 and 2025, respectively. R&D expenses increased to support the continued development of the Company’s pipeline primarily due to increased costs for chemistry, manufacturing, and controls and clinical activity as well as higher personnel-related costs.
General and administrative (G&A) expenses:
G&A expenses were $8.7 million and $8.9 million for the three months ended June 30, 2026 and 2025, respectively. The decrease in G&A expenses is the result of decreased personnel costs, primarily related to share-based compensation and decreased professional service costs, offset by increased office, facilities and software costs and expenses associated with operating as a public company.
Net loss:
Net loss was $24.8 million and $21.8 million, or $0.74 and $4.93 per basic and diluted share, for the three months ended June 30, 2026 and 2025, respectively.
Shares outstanding:
As of June 30, 2026, Crescent had approximately 33.5 million ordinary shares and ordinary share equivalents issued and outstanding, including ordinary shares underlying pre-funded warrants and non-voting convertible preferred stock. Pro forma, Crescent had 43.5 million ordinary shares and ordinary share equivalents issued and outstanding as of June 30, 2026, which includes an additional 9.9 million ordinary shares and ordinary shares underlying pre-funded warrants issued pursuant to the July 2026 public offering.
About Crescent Biopharma
Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates (ADCs). By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit
www.crescentbiopharma.com
and follow the Company on
LinkedIn
and
X
.
Forward-Looking Statements
Certain statements in this press release, other than purely historical information, may constitute "forward-looking statements" within the meaning of the federal securities laws, including for purposes of the "safe harbor" provisions under the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements relating to Crescent’s expectations, beliefs, or strategies regarding the future of its pipeline and business including, without limitation: statements regarding the strategic partnership with Kelun-Biotech, including the potential synergies and benefits of the partnership; the expected benefits or opportunities with respect to CR-001, CR-002, and CR-003, including the expected timelines of regulatory filings and the acceptance thereof, initiation of clinical trials and availability of initial clinical data; the potential for CR-001 to replicate preclinical demonstration of cooperative pharmacology and
in vivo
anti-tumor activity in clinical trials; the Phase 1/2 trial design and indication selection for CR-001; the Phase 2 combination trial for CR-001 and sac-TMT; the potential for CR-002, and CR-003 to act as single agents and in combination with CR-001; and Crescent’s anticipated cash runway. Forward-looking statements generally relate to future events or future financial or operating performance. The words “believe,” “may,” “will,” “potentially,” “estimate,” “continue,” “anticipate,” “predict,” “target,” “intend,” “could,” “would,” “should,” “project,” “plan,” “expect and similar expressions may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements are based on current expectations and beliefs concerning future developments and their potential effects and involve a number of risks, uncertainties or other assumptions that may cause actual performance to be materially different from those expressed or implied by these forward-looking statements. Risks and uncertainties include, but are not limited to: the expected benefits of, and opportunities related to, the strategic partnership between Crescent and Kelun-Biotech may not be realized or may take longer to realize than anticipated; Crescent’s limited operating history, including with respect to clinical trials; Crescent’s historical losses and any future ability to generate revenue; Crescent’s ability to raise capital to support its business plans; risks associated with clinical development and regulatory approval; risks related to Crescent’s intellectual property; Crescent’s reliance on third parties, including to help develop its product candidates, run its clinical trials, and manufacture its product candidates; significant disruptions of information technology systems or breaches of data security, litigation and regulatory risks; risks related to the current macroeconomic environment, including fluctuating interest rates, barriers to trade, changes to fiscal and monetary policy or government budget dynamics, geopolitical factors, including the ongoing conflicts in Iran and between Russia and Ukraine and the responses thereto, and supply chain disruptions, as well as those factors more fully described in Crescent’s most recent filings with the Securities and Exchange Commission (including its Quarterly Report on Form 10-Q), and Crescent’s other filings with the Securities and Exchange Commission. Should one or more of these risks or uncertainties materialize, or should any of Crescent’s assumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. Forward-looking statements in this press release speak only as of the date they are made and are qualified in their entirety by reference to the cautionary statements herein. Except as required by law, Crescent does not undertake or accept any duty to release publicly any updates or revisions to any forward-looking statements.
Crescent Biopharma, Inc.
Condensed Consolidated Statements of Operations
(in thousands, except share and per share data)
(Unaudited)
Three Months Ended June 30, 2026
Six Months Ended June 30, 2026
Three Months Ended June 30, 2025
Six Months Ended June 30, 2025
License agreement revenue
$
—
$
1,039
$
—
$
—
Operating expenses
Research and development
19,391
37,294
12,081
22,708
General and administrative
8,743
16,608
8,949
12,547
Total operating expenses
28,134
53,902
21,030
35,255
Other income
1,770
1,770
—
—
Loss from operations
(26,364
)
(51,093
)
(21,030
)
(35,255
)
Other income (expense)
1,527
2,973
(760
)
(1,683
)
Net loss and comprehensive loss
$
(24,837
)
$
(48,120
)
$
(21,790
)
$
(36,938
)
Net loss per share attributable to ordinary shareholders, basic and diluted
$
(0.74
)
$
(1.44
)
$
(4.93
)
$
(14.11
)
Net loss per share attributable to Series A non-voting convertible preferred shareholders, basic and diluted
$
(743.25
)
$
(1,442.56
)
$
(4,930.97
)
$
(14,104.90
)
Weighted-average ordinary shares outstanding used in computing net loss per share to ordinary shareholders, basic and diluted
30,532,234
30,465,395
3,856,925
2,331,339
Weighted-average Series A non-voting convertible preferred shares outstanding used in computing net loss per share to Series A non-voting convertible preferred shareholders, basic and diluted
2,890
2,890
565
286
Summary Balance Sheet Data
(in thousands)
(Unaudited)
June 30, 2026
December 31, 2025
Assets
Cash
$
171,593
$
213,192
Other assets
11,165
27,101
Total Assets
$
182,758
$
240,293
Liabilities and Shareholders' Equity
Liabilities
$
19,503
$
37,281
Shareholders' equity
163,255
203,012
Total liabilities and shareholders' equity
$
182,758
$
240,293
Contacts
Investors
Amy Reilly
Chief Communications Officer
amy.reilly@crescentbiopharma.com
617-465-0586
Media
Jenna Poist
Director, Corporate Communications
jenna.poist@crescentbiopharma.com
781-671-5019

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