SPRC

Scisparc Ltd
NASDAQHEALTHCAREBIOTECHNOLOGY

Key Statistics

Market Cap
$3.03M
P/E Ratio
0.05
EPS
$98.07
Beta
2.44
52W High
$63.90
52W Low
$2.98
50-Day MA
$5.94
200-Day MA
$7.01
Dividend Yield
—
Profit Margin
0.00%
Forward P/E
—
PEG Ratio
—

About Scisparc Ltd

SciSparc Ltd., a specialized clinical-stage pharmaceutical company, develops drugs based on cannabinoid molecules. The company is headquartered in Tel Aviv, Israel.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)856,000
Gross Profit (TTM)631,000
EBITDA$-8.53M
Operating Margin-849.00%
Return on Equity-178.40%
Return on Assets-60.70%
Revenue/Share (TTM)$6.89
Book Value$11.60
Price-to-Book0.69
Price-to-Sales (TTM)3.54
EV/Revenue174.58
EV/EBITDA1.21
Quarterly Earnings Growth (YoY)0.00%
Quarterly Revenue Growth (YoY)-34.50%
Shares Outstanding580,970
Float553,660
% Insiders0.00%
% Institutions9.38%

Historical Volatility

HV 10-Day
—
HV 20-Day
—
HV 30-Day
—
HV 60-Day
—
HV Rank
—

Latest News

SciSparc Subsidiary NeuroThera Labs Pursues FDA Orphan Drug Designation for Adult Tourette Syndrome Drug; Engages Government and Public Affairs Firm RK Strategies

This strategic engagement is designed to strengthen NeuroThera's U.S. market position, visibility among key U.S. federal stakeholders, reinforce the clinical and public ‑ health importance of advancing new treatment options for adult Tourette Syndrome   TEL AVIV, Israel – TheNewswire - September 2, 2026 - SciSparc Ltd. (Nasdaq: SPRC) (“Company” or “SciSparc”), today announced that its subsidiary, NeuroThera Labs Inc. (TSXV: NTLX) ("NeuroThera"), a clinical-stage pharmaceutical company focused on developing novel treatments for central nervous system disorders, today announced that it is pursuing U.S. Food and Drug Administration (“FDA”) Orphan Drug Designation covering SCI-110, its drug candidate for the treatment adults with Tourette Syndrome (“TS”), a rare condition that may qualify for Orphan Drug Designation.

TheNewswire9/2/2026Neutral
SciSparc: Subsidiary NeuroThera Labs Pursues FDA Orphan Drug Designation for Adult Tourette Syndrome Drug; Engages Government and Public Affairs Firm RK Strategies

This strategic engagement is designed to strengthen NeuroThera's U.S. market position, visibility among key U.S. federal stakeholders, reinforce the clinical and public ‑ health importance of advancing new treatment options for adult Tourette Syndrome   TEL AVIV, Israel – TheNewswire - September 2, 2026 - SciSparc Ltd. (Nasdaq: SPRC) (“Company” or “SciSparc”), today announced that its subsidiary, NeuroThera Labs Inc. (TSXV: NTLX) ("NeuroThera"), a clinical-stage pharmaceutical company focused on developing novel treatments for central nervous system disorders, today announced that it is pursuing U.S. Food and Drug Administration (“FDA”) Orphan Drug Designation covering SCI-110, its drug candidate for the treatment adults with Tourette Syndrome (“TS”), a rare condition that may qualify for Orphan Drug Designation.

TheNewswire9/2/2026Neutral
SciSparc: Subsidiary NeuroThera Labs Achieves Significant Enrollment Momentum in SCI‑210 Autism Clinical Trial

TEL AVIV, Israel, Aug. 31, 2026 (GLOBE NEWSWIRE) -- SciSparc Ltd. (Nasdaq: SPRC) (“Company” or “SciSparc”), today announced that NeuroThera Labs Inc. (TSXV: NTLX) ("NeuroThera"), a clinical-stage pharmaceutical company focused on developing novel treatments for central nervous system disorders, continued advancement in participant enrollment for the clinical trial assessing NeuroThera's innovative SCI-210 treatment for symptoms associated with autism spectrum disorder (“ASD”).

GlobeNewsWire8/31/2026Neutral
NeuroThera Labs Achieves Significant Enrollment Momentum in SCI‑210 Autism Clinical Trial

Toronto, Ontario, August 31, 2026 – TheNewswire – NeuroThera Labs Inc. (TSXV: NTLX) (the " Company " or " NeuroThera "), a clinical-stage pharmaceutical company and a subsidiary of SciSparc Ltd. (Nasdaq: SPRC), today announced continued advancement in participant enrollment for its clinical trial assessing its innovative SCI-210 treatment for symptoms associated with autism spectrum disorder (“ ASD ”).   The clinical trial, conducted at Soroka Medical Center in Israel, is a double-blind, randomized, placebo-controlled study evaluating the safety and efficacy of SCI-210 in children diagnosed with ASD. To date, 26 children have been enrolled, marking strong progress toward the planned total of 60 children between the ages of five and 18, each of whom will receive treatment over a 20-week period.

TheNewswire8/31/2026Neutral
Neurothera Labs Inc. Announces Share Consolidation

Toronto, Ontario – August 28, 2026 – – TheNewswire - NeuroThera Labs Inc. (TSXV: NTLX) (the " Company " or " NeuroThera "), a clinical-stage biotech company and a subsidiary of SciSparc Ltd. (Nasdaq: SPRC), is pleased to announce that, in accordance with special resolution of shareholders passed on January 8, 2026 (the “ Consolidation Resolution ”), the Company will be implementing a consolidation (the “ Consolidation ”) of the outstanding common shares in the capital of the Company (the “ Common Shares ”) on the basis of one new Common Share (each, a “ Post-Consolidation Share ”) for every fourteen (14) currently outstanding Common Shares (the " Consolidation Ratio "). The Company believes that the increase to the trading price of the Common Shares from effecting the consolidation could potentially and principally broaden the pool of investors that may consider investing or be able to invest in the Company as well as enable the Company to satisfy certain minimum trading price requirements of U.S. and other stock exchanges for a potential listing of the Common Shares.

TheNewswire8/28/2026Neutral
NeuroThera Labs Engages Dr. Reuter Investor Relations

Toronto, Ontario – August 27, 2026 – TheNewswire - NeuroThera Labs Inc. (TSXV: NTLX) (the " Company " or " NeuroThera "), a clinical-stage biotech company and a subsidiary of SciSparc Ltd. (Nasdaq: SPRC), is pleased to announce that it has engaged Dr. Reuter Investor Relations (" Dr. Reuter ") to provide investor awareness and communications services across Germany and the broader European capital markets, effective September 1, 2026.   Dr. Reuter is a recognized European investor relations and financial communications firm with an established network of institutional investors, retail shareholders, and financial media throughout the DACH region and the European Union. The engagement is intended to enhance the Company's visibility among European investors, support market education regarding its clinical research strategy, and strengthen shareholder communications. Dr. Reuter's business address is Tower 185, Friedrich-Ebert-Anlage 35-37, 60327 Frankfurt, Germany, and the firm may be contacted at  e.reuter@dr-reuter.eu .

TheNewswire8/27/2026Neutral

Turn research into an automated options-selling system

Tiblio connects your broker and runs your put-and-call-writing strategy for you — on SPRC and any ticker you trade — then tracks every position and per-strategy win rate.

See how it works

More HEALTHCARE Stocks

Data last updated: 9/26/2026