Skip to main content
CPHINYSE

CHINA PHARMA HOLDINGS, INC.

Biopharma developer (SEC filing verified)·Commercial·Haikou, China·CEO: Ms. Zhilin Li
OncologyImmunologyMetabolicRespiratoryDermatologyHematologyNephrologyGastroenterology

CPHI 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

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · CPHI

China Pharma Holdings, Inc. (CPHI) is a specialty pharmaceutical company focused on developing, manufacturing, and marketing generic and branded drugs for the Chinese market, with a pipeline of late-stage clinical candidates and a history of operating losses.

Key risk: Going concern uncertainty

9.9/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$38.9M

Cash Runway

74.5 mo

Lead Asset

Financial data as of Jun 30, 2026.

Tracking 49 clinical trials · 9 catalysts for CHINA PHARMA HOLDINGS, INC..

AI OverviewAI overview is shown in English only.

China Pharma Holdings, Inc. (CPHI) is a specialty pharmaceutical company focused on developing, manufacturing, and marketing generic and branded drugs for the Chinese market, with a pipeline of late-stage clinical candidates and a history of operating losses.

  • Revenue decreased by 10.6% to $1.93 million for the six months ended June 30, 2026, compared to the same period in 2025 [sec_mda · as of 2026-08-14].
  • Cash and equivalents were $0.3M as of June 30, 2026 [latest reported financials].
  • Net loss was $1.5M for the six months ended June 30, 2026 [latest reported financials].
  • The company has a substantial pipeline of Phase 3 trials with topline results expected between December 2026 and June 2029 [upcoming catalysts].
  • The company has a going concern qualification and relies on CEO advances for working capital [sec_mda · as of 2026-04-01].

What works

  • Revenue from CNS Cerebral & Cardio Vascular products increased 34% to $1.02M for the six months ended June 30, 2026, becoming the largest revenue contributor [sec_mda · as of 2026-08-14].
  • The company has multiple Phase 3 registrational trials underway for drugs such as lisaftoclax (APG-2575) and olverembatinib, with topline data expected through 2029 [upcoming catalysts].
  • Shareholders' equity stood at $22.7M as of June 30, 2026, providing a capital base to support operations and clinical development [latest reported financials].

What to weigh

  • Revenue declined 10.6% year-over-year for the six months ended June 30, 2026, driven by a 42% drop in Anti-Viral/Infection & Respiratory product sales [sec_mda · as of 2026-08-14].
  • The company has a going concern qualification, with substantial doubt about its ability to continue as a going concern [sec_mda · as of 2026-04-01].
  • Cash and equivalents were only $0.3M as of June 30, 2026, and the company relies on CEO advances and potential debt/equity financing for liquidity [latest reported financials] [sec_mda · as of 2026-04-01].
  • Net loss was $1.5M for the six months ended June 30, 2026, with accumulated deficits and ongoing operating losses [latest reported financials].

From the filings

Quoted directly from source documents.

  • Revenue decreased by 10.6% to $1.93 million for the six months ended June 30, 2026.

    Revenue decreased by 10.6% to $1.93 million for the six months ended June 30, 2026, compared to $2.16 million for the same period in 2025.

    SEC MD&A · August 14, 2026

  • The company has a going concern qualification.

    This raises substantial doubt about the Company's ability to continue as a going concern.

    SEC MD&A · April 1, 2026

Catalyst timeline

  • 2026-12-31 · Phase3_ToplineTopline results from a randomized, double-blind, placebo-controlled Phase III study expected.
  • 2027-03-31 · Phase3_Topline · asp2215Topline results from a Phase 3 open-label study of ASP2215 versus salvage chemotherapy expected.
  • 2027-10-31 · Phase3_Topline · lisaftoclaxTopline results from a global, open-label, randomized Phase 3 registrational study of lisaftoclax (APG-2575) expected.
  • 2028-07-01 · Phase3_ToplineTopline results from a Phase III randomized, double-blind, placebo-controlled study expected.
  • 2028-08-19 · Phase3_ToplineTopline results from a multi-centre, randomized, placebo-controlled, double-blind trial expected.
  • 2028-12-31 · Phase3_Topline · enzalutamideTopline results from the China ARCHES Phase 3 study of enzalutamide expected.
  • 2029-03-26 · Phase3_Topline · apg-2575Topline results from a global, multicenter, randomized, double-blind Phase 3 pivotal study of APG-2575 expected.
  • 2029-06-30 · Phase3_Topline · olverembatinibTopline results from a pivotal registrational Phase 3 study of olverembatinib combined with chemotherapy expected.
Risks & what to watch (4)

Key risks

  • Going concern uncertaintySubstantial doubt about ability to continue as a going concern [sec_mda · as of 2026-04-01]
  • Low cash reservesOnly $0.3M cash as of June 30, 2026, requiring external financing [latest reported financials]
  • Revenue declineRevenue fell 10.6% in H1 2026 vs H1 2025, with key segment dropping 42% [sec_mda · as of 2026-08-14]
  • Clinical trial failure riskMultiple Phase 3 trials may fail, impacting pipeline value and financing [upcoming catalysts]

What to watch

  • Phase 3 topline results for multiple candidates starting December 2026, which could significantly impact the company's valuation and financing prospects [upcoming catalysts].
  • Ability to secure additional debt or equity financing to address low cash reserves and going concern issues [sec_mda · as of 2026-04-01].
  • Revenue trends in CNS/Cardio Vascular and Anti-Viral segments, which are key to near-term financial performance [sec_mda · as of 2026-08-14].

Sources: SEC MD&A · Generated August 28, 2026 · How we verify sources →

Run CHINA PHARMA HOLDINGS, INC. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available CHINA PHARMA HOLDINGS, INC. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

No clinical pipeline tracked — this score reflects financial & catalyst signals only.

Cash Runway10.0

74.5 months

Financial Health9.6

D/E 0.24 · 0% dilution

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum10.0

9 upcoming, next in ~123d

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Catalysts

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

4

Total value held

$15K

Short Interest

as of May 20, 2026
% of float
0.0%
Days to cover
0.3
Shares short
6,992
Daily short volume (Jul 8, 2026)
4.9%

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 →

CPHI short interest

Governance

Frequently asked questions

What is the AI investment thesis for CHINA PHARMA HOLDINGS, INC.?

China Pharma Holdings, Inc. (CPHI) is a specialty pharmaceutical company focused on developing, manufacturing, and marketing generic and branded drugs for the Chinese market, with a pipeline of late-stage clinical candidates and a history of operating losses.

What is CHINA PHARMA HOLDINGS, INC.'s next catalyst?

CHINA PHARMA HOLDINGS, INC.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A Randomized, Double-blind, Placebo-controlled Phase III Clinical Study to Evaluate the Efficacy and" — expected December 31, 2026.

Who is the CEO of CHINA PHARMA HOLDINGS, INC.?

Ms. Zhilin Li is the chief executive officer of CHINA PHARMA HOLDINGS, INC. (CPHI).

Where is CHINA PHARMA HOLDINGS, INC. headquartered?

CHINA PHARMA HOLDINGS, INC. (CPHI) is headquartered in Haikou, China.

What therapeutic areas does CHINA PHARMA HOLDINGS, INC. focus on?

CHINA PHARMA HOLDINGS, INC. develops therapies across Oncology, Immunology, Metabolic, Respiratory, Dermatology, Hematology, Nephrology, Gastroenterology.

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.