Recent Updates
Recently added Catalysts

SSS68

Phase 1

Healthy | Small molecule | Other |Sunshine Biopharma Inc.|Last Updated: May 26, 2026

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLEDBiomarker
Total Trials1
Total Enrollment50

FDA Designations

No designations recorded

Clinical trial landscape

SSS68 · 1 trial · 1 indication

Phase 1 1
NCT07606976A Study of SSS68 Following a Single Subcutaneous Administration in Healthy Adult ParticipantsHealthy
NOT YET_RECRUITING50 Analytics
PHASE1NOT YET_RECRUITING
A Study of SSS68 Following a Single Subcutaneous Administration in Healthy Adult Participants
HealthyUnlock trial analytics

Study Endpoints

Primary Endpoints

Overall Summary of Treatment Emergent Adverse Events
Baseline to day 113

The number of adverse events (AEs), serious adverse events (SAEs), and drug related adverse events following administration of SSS68.

Secondary Endpoints

Maximum Observed Serum Concentration (Cmax)
0, 2, 6, and 12 hours post-dose, Day 2, 3, 4, 6, 8, 15, 22, 29, 43, 57, 85, and 113
Time to Reach Maximum Observed Serum Concentration (Tmax)
0, 2, 6, and 12 hours post-dose, Day 2, 3, 4, 6, 8, 15, 22, 29, 43, 57, 85, and 113
Terminal half-life (t1/2)
0, 2, 6, and 12 hours post-dose, Day 2, 3, 4, 6, 8, 15, 22, 29, 43, 57, 85, and 113
Unlock Study Endpoints

Study Design & Arms

AllocationRANDOMIZED
MaskingTRIPLE
ModelSEQUENTIAL
PurposeOTHER

Treatment Arms

ArmTypeDescription
SSS68EXPERIMENTALSSS68 at doses ranging from 2 mg up to 1200 mg
PlaceboPLACEBO_COMPARATORMatching placebo

Interventions

NameTypeDescription
SSS68DRUGA single dose of SSS68 will be administered SC on Day 1.
PlaceboDRUGA single dose of placebo will be administered SC on Day 1.
Unlock Study Design Details

Eligibility Criteria

Age Range18 Years to 45 Years
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: 1. Able to understand and comply with protocol requirements, voluntarily participate in the trial and sign a written informed consent form (ICF). 2. Male or female participants aged 18-45 years (inclusive) when signing the ICF. 3. Male participants with body weight ≥ 50 kg, and ...

Countries:China
Unlock Eligibility Criteria

Frequently asked questions about SSS68

What is SSS68 used for?

SSS68 is an investigational small molecule being studied for use in healthy adult participants. It is currently in a Phase 1 clinical trial that evaluates the drug following a single subcutaneous administration. The study is designed to assess the drug's effects in a controlled setting with healthy volunteers.

Who makes SSS68?

SSS68 is being developed by Sunshine Biopharma Inc., a biopharmaceutical company traded on the stock exchange under the ticker symbol SBFM. The company is conducting a Phase 1 clinical trial to evaluate the safety and tolerability of SSS68 in healthy adult participants.

What phase is SSS68 in?

SSS68 is currently in Phase 1 of clinical development. It is an investigational drug that has not yet been approved by regulatory authorities. The ongoing Phase 1 trial is designed to evaluate the drug's safety, tolerability, and pharmacokinetics following a single subcutaneous administration in healthy participants.

What clinical trials is SSS68 in?

SSS68 is being studied in a Phase 1 clinical trial registered as NCT07606976. The trial is titled 'A Study of SSS68 Following a Single Subcutaneous Administration in Healthy Adult Participants' and is planned to enroll 50 participants in China. The study is randomized, double-blind, and placebo-controlled, and it is currently not yet recruiting.

Is SSS68 FDA approved?

SSS68 is not FDA approved. It is an investigational drug currently in Phase 1 clinical development. The drug is being studied in a clinical trial to evaluate its safety and tolerability in healthy participants, but it has not yet received regulatory approval for any use.