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SRZNNasdaq

Surrozen Inc.

Biopharma developer (SEC filing verified)·Phase 1·South San Francisco, CA, United States·CEO: Mr. Craig C. Parker M.B.A.
OphthalmologyInfectious Disease

SRZN evidence brief

What we can confirm

BioSniper Score:
3.5 / 10
Market Cap:
$223.3M
Lead Asset:
szn-043 (Phase 1)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $223.3M · Lead Asset: szn-043 (Phase 1)
BioSniper AIPage evidence connected

Prepared research question

What matters most for SRZN—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · SRZN

Surrozen Inc. (SRZN) is a biotechnology company focused on developing Wnt-pathway-based therapeutics for ophthalmic diseases, with lead candidates SZN-8141 and SZN-8143 targeting retinal vascular conditions and a partnership with Boehringer Ingelheim for SZN-413.

Key risk: Negative equity and accumulated losses

3.5/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$223.3M

Cash Runway

—

Lead Asset

szn-043 (Phase 1)

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 1 clinical trial · 1 catalyst for Surrozen Inc..

AI OverviewAI overview is shown in English only.

Surrozen Inc. (SRZN) is a biotechnology company focused on developing Wnt-pathway-based therapeutics for ophthalmic diseases, with lead candidates SZN-8141 and SZN-8143 targeting retinal vascular conditions and a partnership with Boehringer Ingelheim for SZN-413.

  • Surrozen reported cash & equivalents of $102.0M, total revenue of $5.0M, net income of $50.2M, and shareholders' equity of -$218.7M as of 2026-06-30 [sec].
  • The company received FDA clearance for its IND application for SZN-8141 on October 2, 2026, enabling clinical development for diabetic macular edema [news · 2026-10-02].
  • Boehringer Ingelheim achieved a research milestone for SZN-413 in March 2026, triggering a $5.0 million payment to Surrozen, following a $10.0 million milestone in September 2024 [sec_mda · as of 2026-05-06].
  • Surrozen expects to present retinal vascular research on SZN-8141 at the 2026 ARVO Annual Meeting and has scheduled a Phase 1 trial start for SZN-8141 on 2026-10-30 [news · 2026-03-23] [catalyst].
  • The company has incurred net losses since inception, with an accumulated deficit of $604.6 million as of 2026-08-06 [sec_mda · as of 2026-08-06].

What works

  • Surrozen has a partnership with Boehringer Ingelheim for SZN-413, which has already generated $15.0 million in milestone payments, indicating external validation of its platform [sec_mda · as of 2026-05-06].
  • The company has a cash position of $102.0M as of 2026-06-30, which management believes is sufficient to fund operations for at least 12 months, with potential additional $95.1M from a PIPE upon IND clearance [sec] [sec_mda · as of 2026-08-06].
  • Surrozen has advanced two lead candidates (SZN-8141 and SZN-8143) in retinal vascular disease, with SZN-8141 receiving FDA IND clearance and entering clinical development [news · 2026-10-02].

What to weigh

  • Surrozen has a negative shareholders' equity of -$218.7M and an accumulated deficit of $604.6M, reflecting sustained net losses since inception [sec] [sec_mda · as of 2026-08-06].
  • The company's future capital requirements are uncertain and depend on multiple factors including clinical trial costs, regulatory approvals, and milestone payments, with a risk of using available capital sooner than expected [sec_mda · as of 2026-08-06].
  • Surrozen's revenue is minimal ($5.0M as of 2026-06-30) and primarily from milestone payments, with no approved products generating commercial sales [sec].

From the filings

Quoted directly from source documents.

  • FDA clearance of IND for SZN-8141

    “On October 2, 2026, Surrozen, Inc. (Surrozen) announced U.S. Food and Drug Administration (FDA) clearance of our Investigational New Drug (IND) application for SZN-8141”

    News · October 2, 2026

  • Boehringer Ingelheim milestone payment of $5.0 million

    “In March 2026, Boehringer Ingelheim achieved a research milestone, reflecting a positive outcome of the IND-enabling GLP toxicology study. We received the research milestone payment of $5.0 million from Boehringer Ingelheim in April 2026.”

    SEC MD&A · May 6, 2026

  • Accumulated deficit of $604.6 million

    “deficit of $604.6 million.”

    SEC MD&A · August 6, 2026

Catalyst timeline

  • 2026-10-30 · Phase1_Start — First-in-human trial to evaluate safety, tolerability, PK, PD, and clinical outcomes of SZN-8141 in diabetic macular edema.
Risks & what to watch (3)›

Key risks

  • Negative equity and accumulated losses — Shareholders' equity of -$218.7M and accumulated deficit of $604.6M indicate sustained financial losses since inception [sec] [sec_mda · as of 2026-08-06].
  • Uncertain capital runway — Future funding depends on clinical progress, regulatory outcomes, and milestones; risk of using capital sooner than expected [sec_mda · as of 2026-08-06].
  • Minimal revenue and no approved products — Revenue of $5.0M is milestone-based; no commercial sales from approved products [sec].

What to watch

  • Phase 1 trial start for SZN-8141 in diabetic macular edema on 2026-10-30 [catalyst].
  • Presentation of retinal vascular research on SZN-8141 at the 2026 ARVO Annual Meeting [news · 2026-03-23].
  • Potential receipt of $95.1M from the second closing of the 2025 PIPE, contingent on IND clearance before October 31, 2026 [sec_mda · as of 2026-08-06].
  • Progress of SZN-8143 and any further milestones from the Boehringer Ingelheim collaboration [sec_mda · as of 2026-05-06].

Sources: News · SEC MD&A · Generated October 6, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health3.5

Net income $50M

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth4.6

2 candidates

Catalyst Momentum4.0

1 upcoming, next in ~16d

Insider Signal1.5

0 buys · 5 sells (180d)

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

58

Total value held

$274.3M

Showing top 10 of 58 institutional holders of Surrozen Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 22, 2026
% of float
9.0%
Days to cover
4.3
Shares short
565,307
Daily short volume (Jun 4, 2026)
38.3%

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

SRZN short interest

Governance

Frequently asked questions

What is the AI investment thesis for Surrozen Inc.?

Surrozen Inc. (SRZN) is a biotechnology company focused on developing Wnt-pathway-based therapeutics for ophthalmic diseases, with lead candidates SZN-8141 and SZN-8143 targeting retinal vascular conditions and a partnership with Boehringer Ingelheim for SZN-413.

What is Surrozen Inc.'s lead drug candidate?

Surrozen Inc.'s most advanced tracked candidate is szn-043 (Phase 1) for severe alcohol-associated hepatitis.

What is Surrozen Inc.'s next catalyst?

Surrozen Inc.'s next tracked catalyst is a Phase1_Start event — "Phase1_Start: A First-in-human, Prospective Trial to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Clinical Outcomes of SZN-8141 in Diabetic Macular Edema" — expected October 30, 2026.

Who is the CEO of Surrozen Inc.?

Mr. Craig C. Parker M.B.A. is the chief executive officer of Surrozen Inc. (SRZN).

Where is Surrozen Inc. headquartered?

Surrozen Inc. (SRZN) is headquartered in South San Francisco, CA, United States.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.