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SBFMNasdaqdelisted

SUNSHINE BIOPHARMA INC.

Biopharma developer (SEC filing verified)·Phase 3·Fort Lauderdale, FL, United States·CEO: Dr. Steve N. Slilaty Ph.D.
OncologyImmunologyOphthalmologyDermatology

SBFM evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

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

What to watch

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BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · SBFM

Sunshine Biopharma Inc. (SBFM) is a pharmaceutical company focused on the research, development and commercialization of drugs for the treatment of various forms of cancer, with lead compound Adva-27a. As of June 30, 2026, the company reported cash of $13.7M, total revenue of $9.3M, and a net loss of $1.6M.

Key risk: Going concern uncertainty

6.2/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$4.5M

Cash Runway

61.5 mo

Lead Asset

adva-27a (Preclinical)

Next Catalyst

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 11 clinical trials for SUNSHINE BIOPHARMA INC..

AI OverviewAI overview is shown in English only.

Sunshine Biopharma Inc. (SBFM) is a pharmaceutical company focused on the research, development and commercialization of drugs for the treatment of various forms of cancer, with lead compound Adva-27a. As of June 30, 2026, the company reported cash of $13.7M, total revenue of $9.3M, and a net loss of $1.6M.

  • Cash and equivalents of $13.7M as of 2026-06-30 [sec].
  • Total revenue of $9.3M as of 2026-06-30 [sec].
  • Net loss of $1.6M as of 2026-06-30 [sec].
  • Shareholders' equity of $23.5M as of 2026-06-30 [sec].
  • Lead compound Adva-27a is a multi-purpose anti-tumor compound [sec · filed 2014-03-19].

What works

  • The company has a lead compound, Adva-27a, which is a multi-purpose anti-tumor compound under development [sec · filed 2014-03-19].
  • As of June 30, 2026, the company had $13.7M in cash and equivalents, providing some near-term liquidity [sec].

What to weigh

  • The company has historically incurred significant net losses and an accumulated deficit of $5,494,149 as of December 31, 2013 [sec · filed 2014-03-19].
  • The company has not generated any material revenues historically and expects to require additional funding to fully implement its business plan [sec · filed 2014-03-19].
  • The company's independent registered public accounting firm included a going concern explanatory paragraph in its report [sec · filed 2014-03-19].
  • The company faces extensive FDA regulatory requirements and delays in clinical trials could adversely affect its ability to generate revenues [sec · filed 2014-03-19].

From the filings

Quoted directly from source documents.

  • The company has incurred significant net losses and an accumulated deficit.

    We have incurred an accumulated deficit of $5,494,149 as of December 31, 2013.

    SEC filings · March 19, 2014

  • The company has not generated any revenues historically.

    To date, we have not generated any revenues and we do not anticipate generating any revenues in the near term, if ever.

    SEC filings · March 19, 2014

  • The company's auditor expressed substantial doubt about its ability to continue as a going concern.

    The paragraph stated that we do not have sufficient cash on-hand or other funding available to meet our obligations and sustain our operations, which raises substantial doubt about our ability to continue as a going concern.

    SEC filings · March 19, 2014

Catalyst timeline

  • 2026-12-31 · Phase1_Start · clifutinib — Phase 1 Start: The Drug-Drug Interaction Study of ClifutinibInitiation of Phase 1 clinical trial for clifutinib to evaluate drug-drug interactions.
  • 2027-11-01 · Phase3_Topline — Phase 3 Topline: A Phase II/III ,Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled, AdaptiveTopline results from a Phase II/III adaptive trial expected.
  • 2027-11-01 · Phase3_Topline · mitizodone — Phase 3 Topline: A Phase II/III ,Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled, AdaptiveTopline results for mitizodone from a Phase II/III adaptive trial expected.
  • 2027-12-01 · Phase3_Topline — Phase 3 Topline: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study on the Efficacy and SafetTopline results from a Phase 3 placebo-controlled efficacy and safety study expected.
  • 2028-05-30 · Phase3_Topline — Phase 3 Topline: HEC73543 Versus Salvage Chemotherapy in Relapsed or Refractory FLT3-ITD Acute Myeloid Leukemia: a MuTopline results for HEC73543 in FLT3-ITD AML versus salvage chemotherapy expected.
  • 2029-02-07 · Phase3_Topline — Phase 3 Topline: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Evaluate the EfficacyTopline results from a Phase 3 placebo-controlled efficacy study expected.
  • 2032-02-15 · Phase3_Topline · hec585 — Phase 3 Topline: A Multicenter, Parallel, Randomized, Placebo (Double-blind) and Pirfenidone (Open-label) ControlledTopline results for hec585 from a Phase 3 trial with placebo and pirfenidone control expected.
Risks & what to watch (4)

Key risks

  • Going concern uncertaintyAuditor expressed substantial doubt about ability to continue as a going concern due to insufficient cash [sec · filed 2014-03-19].
  • No revenue historyCompany has not generated any material revenues and does not anticipate near-term revenue [sec · filed 2014-03-19].
  • Regulatory approval delaysFDA approval process is extensive; delays in clinical trials could prevent commercialization [sec · filed 2014-03-19].
  • Dependence on additional financingCompany requires significant additional capital to implement business plan; no assurance of availability [sec · filed 2014-03-19].

What to watch

  • Upcoming Phase 1 start for clifutinib drug-drug interaction study on 2026-12-31 [catalyst].
  • Phase 3 topline data for mitizodone expected on 2027-11-01 [catalyst].
  • Phase 3 topline data for HEC73543 in FLT3-ITD AML expected on 2028-05-30 [catalyst].
  • Phase 3 topline data for hec585 expected on 2032-02-15 [catalyst].

Sources: SEC filings · Generated August 22, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash Runway10.0

61.5 months

Financial Health9.3

D/E 0.22

Pipeline Maturity2.0

Lead: Preclinical

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

10

Total value held

$124K

Short Interest

as of Apr 21, 2026
% of float
2.9%
Days to cover
3.9
Shares short
140,026
Daily short volume
-

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 →

SBFM short interest

Governance

Frequently asked questions

What is the AI investment thesis for SUNSHINE BIOPHARMA INC.?

Sunshine Biopharma Inc. (SBFM) is a pharmaceutical company focused on the research, development and commercialization of drugs for the treatment of various forms of cancer, with lead compound Adva-27a. As of June 30, 2026, the company reported cash of $13.7M, total revenue of $9.3M, and a net loss of $1.6M.

What is SUNSHINE BIOPHARMA INC.'s lead drug candidate?

SUNSHINE BIOPHARMA INC.'s most advanced tracked candidate is adva-27a (Preclinical) for multidrug resistant breast cancer.

Who is the CEO of SUNSHINE BIOPHARMA INC.?

Dr. Steve N. Slilaty Ph.D. is the chief executive officer of SUNSHINE BIOPHARMA INC. (SBFM).

Where is SUNSHINE BIOPHARMA INC. headquartered?

SUNSHINE BIOPHARMA INC. (SBFM) is headquartered in Fort Lauderdale, FL, United States.

What therapeutic areas does SUNSHINE BIOPHARMA INC. focus on?

SUNSHINE BIOPHARMA INC. develops therapies across Oncology, Immunology, Ophthalmology, Dermatology.

925 companies232,681 SEC filings21,419 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.